Canonical Allele Identifier: CA741074981
Gene: SNAP25 HGNC NCBI

Linked Data

dbSNP Id: rs1418382502

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.10245559_10245560del , CM000682.2:g.10245559_10245560del GRCh38
NC_000020.10:g.10226207_10226208del , CM000682.1:g.10226207_10226208del GRCh37
NC_000020.9:g.10174207_10174208del NCBI36
NG_029626.1:g.31731_31732del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706269.1:c.-64+26346_-64+26347del ENSP00000516314.1:n.-64+26346_-64+26347del
ENST00000685131.1:c.-64+7533_-64+7534del ENSP00000508837.1:n.-64+7533_-64+7534del
ENST00000687785.1:c.-64+666_-64+667del ENSP00000510219.1:n.-64+666_-64+667del
ENST00000689077.1:n.393-29870_393-29869del
ENST00000689248.1:n.238+666_238+667del
ENST00000689757.1:c.-108-13798_-108-13797del ENSP00000509312.1:n.-108-13798_-108-13797del
ENST00000689858.1:c.-64+1525_-64+1526del ENSP00000510663.1:n.-64+1525_-64+1526del
ENST00000690099.1:n.393-29870_393-29869del
ENST00000690766.1:n.393-29870_393-29869del
ENST00000690812.1:c.-109+1525_-109+1526del ENSP00000509287.1:n.-109+1525_-109+1526del
ENST00000691161.1:c.-64+18121_-64+18122del ENSP00000510109.1:n.-64+18121_-64+18122del
ENST00000691353.1:c.-262-19920_-262-19919del ENSP00000509759.1:n.-262-19920_-262-19919del
ENST00000691665.1:c.-64+11222_-64+11223del ENSP00000508541.1:n.-64+11222_-64+11223del
ENST00000692411.1:c.-148-15672_-148-15671del ENSP00000508939.1:n.-148-15672_-148-15671del
ENST00000693325.1:c.-64+18121_-64+18122del ENSP00000510558.1:n.-64+18121_-64+18122del
ENST00000693732.1:n.393-29870_393-29869del
ENST00000254976.7:c.-64+26582_-64+26583del MANE Select ENSP00000254976.3:n.-64+26582_-64+26583del
ENST00000254976.6:c.-64+26582_-64+26583del ENSP00000254976.2:n.-64+26582_-64+26583del
ENST00000304886.6:c.-64+26582_-64+26583del ENSP00000307341.2:n.-64+26582_-64+26583del
ENST00000430336.1:c.-64+26346_-64+26347del ENSP00000400720.1:n.-64+26346_-64+26347del
NM_003081.3:c.-64+26582_-64+26583del NP_003072.2:n.-64+26582_-64+26583del
NM_130811.2:c.-64+26582_-64+26583del NP_570824.1:n.-64+26582_-64+26583del
XM_005260808.3:c.-64+26346_-64+26347del XP_005260865.1:n.-64+26346_-64+26347del
XM_005260810.3:c.-64+26346_-64+26347del XP_005260867.1:n.-64+26346_-64+26347del
NM_001322902.1:c.-64+26346_-64+26347del NP_001309831.1:n.-64+26346_-64+26347del
NM_001322903.1:c.-64+11222_-64+11223del NP_001309832.1:n.-64+11222_-64+11223del
NM_001322904.1:c.-64+18121_-64+18122del NP_001309833.1:n.-64+18121_-64+18122del
NM_001322905.1:c.-64+1525_-64+1526del NP_001309834.1:n.-64+1525_-64+1526del
NM_001322906.1:c.-64+7533_-64+7534del NP_001309835.1:n.-64+7533_-64+7534del
NM_001322907.1:c.-64+18121_-64+18122del NP_001309836.1:n.-64+18121_-64+18122del
NM_001322908.1:c.-64+666_-64+667del NP_001309837.1:n.-64+666_-64+667del
NM_001322909.1:c.-108-13798_-108-13797del NP_001309838.1:n.-108-13798_-108-13797del
NM_001322910.1:c.-64+18121_-64+18122del NP_001309839.1:n.-64+18121_-64+18122del
NM_003081.4:c.-64+26582_-64+26583del NP_003072.2:n.-64+26582_-64+26583del
NM_130811.3:c.-64+26582_-64+26583del NP_570824.1:n.-64+26582_-64+26583del
XM_005260808.5:c.-64+26346_-64+26347del XP_005260865.1:n.-64+26346_-64+26347del
XM_017028021.2:c.-64+1525_-64+1526del XP_016883510.1:n.-64+1525_-64+1526del
XM_017028022.1:c.-64+7533_-64+7534del XP_016883511.1:n.-64+7533_-64+7534del
NM_001322902.2:c.-64+26346_-64+26347del NP_001309831.1:n.-64+26346_-64+26347del
NM_001322903.2:c.-64+11222_-64+11223del NP_001309832.1:n.-64+11222_-64+11223del
NM_001322904.2:c.-64+18121_-64+18122del NP_001309833.1:n.-64+18121_-64+18122del
NM_001322905.2:c.-64+1525_-64+1526del NP_001309834.1:n.-64+1525_-64+1526del
NM_001322906.2:c.-64+7533_-64+7534del NP_001309835.1:n.-64+7533_-64+7534del
NM_001322907.2:c.-64+18121_-64+18122del NP_001309836.1:n.-64+18121_-64+18122del
NM_001322908.2:c.-64+666_-64+667del NP_001309837.1:n.-64+666_-64+667del
NM_001322909.2:c.-108-13798_-108-13797del NP_001309838.1:n.-108-13798_-108-13797del
NM_001322910.2:c.-64+18121_-64+18122del NP_001309839.1:n.-64+18121_-64+18122del
NM_003081.5:c.-64+26582_-64+26583del NP_003072.2:n.-64+26582_-64+26583del
NM_130811.4:c.-64+26582_-64+26583del MANE Select NP_570824.1:n.-64+26582_-64+26583del