Canonical Allele Identifier: CA741077320

Gene: SNAP25

Linked Data

• dbSNP Id: rs1304379547
• MyVariant Identifiers: chr20:g.10234333_10234334insT (hg19) ; chr20:g.10253685_10253686insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.10253686dup , CM000682.2:g.10253686dup	GRCh38
NC_000020.10:g.10234334dup , CM000682.1:g.10234334dup	GRCh37
NC_000020.9:g.10182334dup	NCBI36
NG_029626.1:g.39858dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000706269.1:c.-63-21743dup	ENSP00000516314.1:n.-63-21743dup
ENST00000685131.1:c.-64+15660dup	ENSP00000508837.1:n.-64+15660dup
ENST00000687785.1:c.-64+8793dup	ENSP00000510219.1:n.-64+8793dup
ENST00000689077.1:n.393-21743dup
ENST00000689757.1:c.-108-5671dup	ENSP00000509312.1:n.-108-5671dup
ENST00000689858.1:c.-64+9652dup	ENSP00000510663.1:n.-64+9652dup
ENST00000690099.1:n.393-21743dup
ENST00000690766.1:n.393-21743dup
ENST00000690812.1:c.-108-5671dup	ENSP00000509287.1:n.-108-5671dup
ENST00000691161.1:c.-63-21743dup	ENSP00000510109.1:n.-63-21743dup
ENST00000691353.1:c.-262-11793dup	ENSP00000509759.1:n.-262-11793dup
ENST00000691665.1:c.-64+19349dup	ENSP00000508541.1:n.-64+19349dup
ENST00000692411.1:c.-148-7545dup	ENSP00000508939.1:n.-148-7545dup
ENST00000693325.1:c.-63-21743dup	ENSP00000510558.1:n.-63-21743dup
ENST00000693732.1:n.393-21743dup
ENST00000254976.7:c.-63-21743dup MANE Select	ENSP00000254976.3:n.-63-21743dup
ENST00000254976.6:c.-63-21743dup	ENSP00000254976.2:n.-63-21743dup
ENST00000304886.6:c.-63-21743dup	ENSP00000307341.2:n.-63-21743dup
ENST00000430336.1:c.-63-21743dup	ENSP00000400720.1:n.-63-21743dup
NM_003081.3:c.-63-21743dup	NP_003072.2:n.-63-21743dup
NM_130811.2:c.-63-21743dup	NP_570824.1:n.-63-21743dup
XM_005260808.3:c.-63-21743dup	XP_005260865.1:n.-63-21743dup
XM_005260810.3:c.-63-21743dup	XP_005260867.1:n.-63-21743dup
NM_001322902.1:c.-63-21743dup	NP_001309831.1:n.-63-21743dup
NM_001322903.1:c.-64+19349dup	NP_001309832.1:n.-64+19349dup
NM_001322904.1:c.-63-21743dup	NP_001309833.1:n.-63-21743dup
NM_001322905.1:c.-64+9652dup	NP_001309834.1:n.-64+9652dup
NM_001322906.1:c.-64+15660dup	NP_001309835.1:n.-64+15660dup
NM_001322907.1:c.-63-21743dup	NP_001309836.1:n.-63-21743dup
NM_001322908.1:c.-64+8793dup	NP_001309837.1:n.-64+8793dup
NM_001322909.1:c.-108-5671dup	NP_001309838.1:n.-108-5671dup
NM_001322910.1:c.-63-21743dup	NP_001309839.1:n.-63-21743dup
NM_003081.4:c.-63-21743dup	NP_003072.2:n.-63-21743dup
NM_130811.3:c.-63-21743dup	NP_570824.1:n.-63-21743dup
XM_005260808.5:c.-63-21743dup	XP_005260865.1:n.-63-21743dup
XM_017028021.2:c.-64+9652dup	XP_016883510.1:n.-64+9652dup
XM_017028022.1:c.-64+15660dup	XP_016883511.1:n.-64+15660dup
NM_001322902.2:c.-63-21743dup	NP_001309831.1:n.-63-21743dup
NM_001322903.2:c.-64+19349dup	NP_001309832.1:n.-64+19349dup
NM_001322904.2:c.-63-21743dup	NP_001309833.1:n.-63-21743dup
NM_001322905.2:c.-64+9652dup	NP_001309834.1:n.-64+9652dup
NM_001322906.2:c.-64+15660dup	NP_001309835.1:n.-64+15660dup
NM_001322907.2:c.-63-21743dup	NP_001309836.1:n.-63-21743dup
NM_001322908.2:c.-64+8793dup	NP_001309837.1:n.-64+8793dup
NM_001322909.2:c.-108-5671dup	NP_001309838.1:n.-108-5671dup
NM_001322910.2:c.-63-21743dup	NP_001309839.1:n.-63-21743dup
NM_003081.5:c.-63-21743dup	NP_003072.2:n.-63-21743dup
NM_130811.4:c.-63-21743dup MANE Select	NP_570824.1:n.-63-21743dup