Canonical Allele Identifier: CA2396589557

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888307_20888319delinsTCATTCACACACA , CM000684.2:g.20888307_20888319delinsTCATTCACACACA	GRCh38
NC_000022.10:g.21242595_21242607delinsTCATTCACACACA , CM000684.1:g.21242595_21242607delinsTCATTCACACACA	GRCh37
NC_000022.9:g.19572595_19572607delinsTCATTCACACACA	NCBI36
NG_012152.1:g.34304_34316delinsTCATTCACACACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*471_*483delinsTCATTCACACACA MANE Select	ENSP00000215730.6:n.*471_*483delinsTCATTCACACACA
ENST00000215730.11:c.*471_*483delinsTCATTCACACACA	ENSP00000215730.6:n.*471_*483delinsTCATTCACACACA
NM_004782.3:c.*471_*483delinsTCATTCACACACA	NP_004773.1:n.*471_*483delinsTCATTCACACACA
NM_004782.4:c.*471_*483delinsTCATTCACACACA MANE Select	NP_004773.1:n.*471_*483delinsTCATTCACACACA