Canonical Allele Identifier: CA741077249
Gene: SNAP25 HGNC NCBI

Linked Data

dbSNP Id: rs1409716110

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10253475_10253477del , CM000682.2:g.10253475_10253477del GRCh38
NC_000020.10:g.10234123_10234125del , CM000682.1:g.10234123_10234125del GRCh37
NC_000020.9:g.10182123_10182125del NCBI36
NG_029626.1:g.39647_39649del

Transcript Alleles

HGVS Amino-acid change
ENST00000706269.1:c.-63-21954_-63-21952del ENSP00000516314.1:n.-63-21954_-63-21952de...
ENST00000685131.1:c.-64+15449_-64+15451del ENSP00000508837.1:n.-64+15449_-64+15451de...
ENST00000687785.1:c.-64+8582_-64+8584del ENSP00000510219.1:n.-64+8582_-64+8584del
ENST00000689077.1:n.393-21954_393-21952del
ENST00000689757.1:c.-108-5882_-108-5880del ENSP00000509312.1:n.-108-5882_-108-5880de...
ENST00000689858.1:c.-64+9441_-64+9443del ENSP00000510663.1:n.-64+9441_-64+9443del
ENST00000690099.1:n.393-21954_393-21952del
ENST00000690766.1:n.393-21954_393-21952del
ENST00000690812.1:c.-108-5882_-108-5880del ENSP00000509287.1:n.-108-5882_-108-5880de...
ENST00000691161.1:c.-63-21954_-63-21952del ENSP00000510109.1:n.-63-21954_-63-21952de...
ENST00000691353.1:c.-262-12004_-262-12002del ENSP00000509759.1:n.-262-12004_-262-12002...
ENST00000691665.1:c.-64+19138_-64+19140del ENSP00000508541.1:n.-64+19138_-64+19140de...
ENST00000692411.1:c.-148-7756_-148-7754del ENSP00000508939.1:n.-148-7756_-148-7754de...
ENST00000693325.1:c.-63-21954_-63-21952del ENSP00000510558.1:n.-63-21954_-63-21952de...
ENST00000693732.1:n.393-21954_393-21952del
ENST00000254976.7:c.-63-21954_-63-21952del MANE Select ENSP00000254976.3:n.-63-21954_-63-21952de...
ENST00000254976.6:c.-63-21954_-63-21952del ENSP00000254976.2:n.-63-21954_-63-21952de...
ENST00000304886.6:c.-63-21954_-63-21952del ENSP00000307341.2:n.-63-21954_-63-21952de...
ENST00000430336.1:c.-63-21954_-63-21952del ENSP00000400720.1:n.-63-21954_-63-21952de...
NM_003081.3:c.-63-21954_-63-21952del NP_003072.2:n.-63-21954_-63-21952del
NM_130811.2:c.-63-21954_-63-21952del NP_570824.1:n.-63-21954_-63-21952del
XM_005260808.3:c.-63-21954_-63-21952del XP_005260865.1:n.-63-21954_-63-21952del
XM_005260810.3:c.-63-21954_-63-21952del XP_005260867.1:n.-63-21954_-63-21952del
NM_001322902.1:c.-63-21954_-63-21952del NP_001309831.1:n.-63-21954_-63-21952del
NM_001322903.1:c.-64+19138_-64+19140del NP_001309832.1:n.-64+19138_-64+19140del
NM_001322904.1:c.-63-21954_-63-21952del NP_001309833.1:n.-63-21954_-63-21952del
NM_001322905.1:c.-64+9441_-64+9443del NP_001309834.1:n.-64+9441_-64+9443del
NM_001322906.1:c.-64+15449_-64+15451del NP_001309835.1:n.-64+15449_-64+15451del
NM_001322907.1:c.-63-21954_-63-21952del NP_001309836.1:n.-63-21954_-63-21952del
NM_001322908.1:c.-64+8582_-64+8584del NP_001309837.1:n.-64+8582_-64+8584del
NM_001322909.1:c.-108-5882_-108-5880del NP_001309838.1:n.-108-5882_-108-5880del
NM_001322910.1:c.-63-21954_-63-21952del NP_001309839.1:n.-63-21954_-63-21952del
NM_003081.4:c.-63-21954_-63-21952del NP_003072.2:n.-63-21954_-63-21952del
NM_130811.3:c.-63-21954_-63-21952del NP_570824.1:n.-63-21954_-63-21952del
XM_005260808.5:c.-63-21954_-63-21952del XP_005260865.1:n.-63-21954_-63-21952del
XM_017028021.2:c.-64+9441_-64+9443del XP_016883510.1:n.-64+9441_-64+9443del
XM_017028022.1:c.-64+15449_-64+15451del XP_016883511.1:n.-64+15449_-64+15451del
NM_001322902.2:c.-63-21954_-63-21952del NP_001309831.1:n.-63-21954_-63-21952del
NM_001322903.2:c.-64+19138_-64+19140del NP_001309832.1:n.-64+19138_-64+19140del
NM_001322904.2:c.-63-21954_-63-21952del NP_001309833.1:n.-63-21954_-63-21952del
NM_001322905.2:c.-64+9441_-64+9443del NP_001309834.1:n.-64+9441_-64+9443del
NM_001322906.2:c.-64+15449_-64+15451del NP_001309835.1:n.-64+15449_-64+15451del
NM_001322907.2:c.-63-21954_-63-21952del NP_001309836.1:n.-63-21954_-63-21952del
NM_001322908.2:c.-64+8582_-64+8584del NP_001309837.1:n.-64+8582_-64+8584del
NM_001322909.2:c.-108-5882_-108-5880del NP_001309838.1:n.-108-5882_-108-5880del
NM_001322910.2:c.-63-21954_-63-21952del NP_001309839.1:n.-63-21954_-63-21952del
NM_003081.5:c.-63-21954_-63-21952del NP_003072.2:n.-63-21954_-63-21952del
NM_130811.4:c.-63-21954_-63-21952del MANE Select NP_570824.1:n.-63-21954_-63-21952del