Canonical Allele Identifier: CA2655449506

Gene: SNAP29

Linked Data

• gnomAD v4: 22-20888471-A-ATATG

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888471_20888472insTATG , CM000684.2:g.20888471_20888472insTATG	GRCh38
NC_000022.10:g.21242759_21242760insTATG , CM000684.1:g.21242759_21242760insTATG	GRCh37
NC_000022.9:g.19572759_19572760insTATG	NCBI36
NG_012152.1:g.34468_34469insTATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*635_*636insTATG MANE Select	ENSP00000215730.6:n.*635_*636insTATG
ENST00000215730.11:c.*635_*636insTATG	ENSP00000215730.6:n.*635_*636insTATG
NM_004782.3:c.*635_*636insTATG	NP_004773.1:n.*635_*636insTATG
NM_004782.4:c.*635_*636insTATG MANE Select	NP_004773.1:n.*635_*636insTATG