Canonical Allele Identifier: CA2522598221

Gene: SNAP25

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10245246_10245247insGGC , CM000682.2:g.10245246_10245247insGGC	GRCh38
NC_000020.10:g.10225894_10225895insGGC , CM000682.1:g.10225894_10225895insGGC	GRCh37
NC_000020.9:g.10173894_10173895insGGC	NCBI36
NG_029626.1:g.31418_31419insGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706269.1:c.-64+26033_-64+26034insGGC	ENSP00000516314.1:n.-64+26033_-64+26034insGGC
ENST00000685131.1:c.-64+7220_-64+7221insGGC	ENSP00000508837.1:n.-64+7220_-64+7221insGGC
ENST00000687785.1:c.-64+353_-64+354insGGC	ENSP00000510219.1:n.-64+353_-64+354insGGC
ENST00000689077.1:n.393-30183_393-30182insGGC
ENST00000689248.1:n.238+353_238+354insGGC
ENST00000689757.1:c.-108-14111_-108-14110insGGC	ENSP00000509312.1:n.-108-14111_-108-14110insGGC
ENST00000689858.1:c.-64+1212_-64+1213insGGC	ENSP00000510663.1:n.-64+1212_-64+1213insGGC
ENST00000690099.1:n.393-30183_393-30182insGGC
ENST00000690766.1:n.393-30183_393-30182insGGC
ENST00000690812.1:c.-109+1212_-109+1213insGGC	ENSP00000509287.1:n.-109+1212_-109+1213insGGC
ENST00000691161.1:c.-64+17808_-64+17809insGGC	ENSP00000510109.1:n.-64+17808_-64+17809insGGC
ENST00000691353.1:c.-262-20233_-262-20232insGGC	ENSP00000509759.1:n.-262-20233_-262-20232insGGC
ENST00000691665.1:c.-64+10909_-64+10910insGGC	ENSP00000508541.1:n.-64+10909_-64+10910insGGC
ENST00000692411.1:c.-148-15985_-148-15984insGGC	ENSP00000508939.1:n.-148-15985_-148-15984insGGC
ENST00000693325.1:c.-64+17808_-64+17809insGGC	ENSP00000510558.1:n.-64+17808_-64+17809insGGC
ENST00000693732.1:n.393-30183_393-30182insGGC
ENST00000254976.7:c.-64+26269_-64+26270insGGC MANE Select	ENSP00000254976.3:n.-64+26269_-64+26270insGGC
ENST00000254976.6:c.-64+26269_-64+26270insGGC	ENSP00000254976.2:n.-64+26269_-64+26270insGGC
ENST00000304886.6:c.-64+26269_-64+26270insGGC	ENSP00000307341.2:n.-64+26269_-64+26270insGGC
ENST00000430336.1:c.-64+26033_-64+26034insGGC	ENSP00000400720.1:n.-64+26033_-64+26034insGGC
NM_003081.3:c.-64+26269_-64+26270insGGC	NP_003072.2:n.-64+26269_-64+26270insGGC
NM_130811.2:c.-64+26269_-64+26270insGGC	NP_570824.1:n.-64+26269_-64+26270insGGC
XM_005260808.3:c.-64+26033_-64+26034insGGC	XP_005260865.1:n.-64+26033_-64+26034insGGC
XM_005260810.3:c.-64+26033_-64+26034insGGC	XP_005260867.1:n.-64+26033_-64+26034insGGC
NM_001322902.1:c.-64+26033_-64+26034insGGC	NP_001309831.1:n.-64+26033_-64+26034insGGC
NM_001322903.1:c.-64+10909_-64+10910insGGC	NP_001309832.1:n.-64+10909_-64+10910insGGC
NM_001322904.1:c.-64+17808_-64+17809insGGC	NP_001309833.1:n.-64+17808_-64+17809insGGC
NM_001322905.1:c.-64+1212_-64+1213insGGC	NP_001309834.1:n.-64+1212_-64+1213insGGC
NM_001322906.1:c.-64+7220_-64+7221insGGC	NP_001309835.1:n.-64+7220_-64+7221insGGC
NM_001322907.1:c.-64+17808_-64+17809insGGC	NP_001309836.1:n.-64+17808_-64+17809insGGC
NM_001322908.1:c.-64+353_-64+354insGGC	NP_001309837.1:n.-64+353_-64+354insGGC
NM_001322909.1:c.-108-14111_-108-14110insGGC	NP_001309838.1:n.-108-14111_-108-14110insGGC
NM_001322910.1:c.-64+17808_-64+17809insGGC	NP_001309839.1:n.-64+17808_-64+17809insGGC
NM_003081.4:c.-64+26269_-64+26270insGGC	NP_003072.2:n.-64+26269_-64+26270insGGC
NM_130811.3:c.-64+26269_-64+26270insGGC	NP_570824.1:n.-64+26269_-64+26270insGGC
XM_005260808.5:c.-64+26033_-64+26034insGGC	XP_005260865.1:n.-64+26033_-64+26034insGGC
XM_017028021.2:c.-64+1212_-64+1213insGGC	XP_016883510.1:n.-64+1212_-64+1213insGGC
XM_017028022.1:c.-64+7220_-64+7221insGGC	XP_016883511.1:n.-64+7220_-64+7221insGGC
NM_001322902.2:c.-64+26033_-64+26034insGGC	NP_001309831.1:n.-64+26033_-64+26034insGGC
NM_001322903.2:c.-64+10909_-64+10910insGGC	NP_001309832.1:n.-64+10909_-64+10910insGGC
NM_001322904.2:c.-64+17808_-64+17809insGGC	NP_001309833.1:n.-64+17808_-64+17809insGGC
NM_001322905.2:c.-64+1212_-64+1213insGGC	NP_001309834.1:n.-64+1212_-64+1213insGGC
NM_001322906.2:c.-64+7220_-64+7221insGGC	NP_001309835.1:n.-64+7220_-64+7221insGGC
NM_001322907.2:c.-64+17808_-64+17809insGGC	NP_001309836.1:n.-64+17808_-64+17809insGGC
NM_001322908.2:c.-64+353_-64+354insGGC	NP_001309837.1:n.-64+353_-64+354insGGC
NM_001322909.2:c.-108-14111_-108-14110insGGC	NP_001309838.1:n.-108-14111_-108-14110insGGC
NM_001322910.2:c.-64+17808_-64+17809insGGC	NP_001309839.1:n.-64+17808_-64+17809insGGC
NM_003081.5:c.-64+26269_-64+26270insGGC	NP_003072.2:n.-64+26269_-64+26270insGGC
NM_130811.4:c.-64+26269_-64+26270insGGC MANE Select	NP_570824.1:n.-64+26269_-64+26270insGGC