Canonical Allele Identifier: CA2655449856

Gene: SNAP29

Linked Data

• gnomAD v4: 22-20889351-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20889351A>C , CM000684.2:g.20889351A>C	GRCh38
NC_000022.10:g.21243639A>C , CM000684.1:g.21243639A>C	GRCh37
NC_000022.9:g.19573639A>C	NCBI36
NG_012152.1:g.35348A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000215730.12:c.*1515A>C MANE Select	ENSP00000215730.6:n.*1515A>C
ENST00000215730.11:c.*1515A>C	ENSP00000215730.6:n.*1515A>C
NM_004782.3:c.*1515A>C	NP_004773.1:n.*1515A>C
NM_004782.4:c.*1515A>C MANE Select	NP_004773.1:n.*1515A>C