Canonical Allele Identifier: CA2655449515

Gene: SNAP29

Linked Data

• gnomAD v4: 22-20888476-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888476_20888477insA , CM000684.2:g.20888476_20888477insA	GRCh38
NC_000022.10:g.21242764_21242765insA , CM000684.1:g.21242764_21242765insA	GRCh37
NC_000022.9:g.19572764_19572765insA	NCBI36
NG_012152.1:g.34473_34474insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*640_*641insA MANE Select	ENSP00000215730.6:n.*640_*641insA
ENST00000215730.11:c.*640_*641insA	ENSP00000215730.6:n.*640_*641insA
NM_004782.3:c.*640_*641insA	NP_004773.1:n.*640_*641insA
NM_004782.4:c.*640_*641insA MANE Select	NP_004773.1:n.*640_*641insA