Canonical Allele Identifier: CA2655449392

Gene: SNAP29

Linked Data

• gnomAD v4: 22-20888351-A-ACACACACACACACACC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888356_20888357insACACACACACCCACAC , CM000684.2:g.20888356_20888357insACACACACACCCACAC	GRCh38
NC_000022.10:g.21242644_21242645insACACACACACCCACAC , CM000684.1:g.21242644_21242645insACACACACACCCACAC	GRCh37
NC_000022.9:g.19572644_19572645insACACACACACCCACAC	NCBI36
NG_012152.1:g.34353_34354insACACACACACCCACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*520_*521insACACACACACCCACAC MANE Select	ENSP00000215730.6:n.*520_*521insACACACACACCCACAC
ENST00000215730.11:c.*520_*521insACACACACACCCACAC	ENSP00000215730.6:n.*520_*521insACACACACACCCACAC
NM_004782.3:c.*520_*521insACACACACACCCACAC	NP_004773.1:n.*520_*521insACACACACACCCACAC
NM_004782.4:c.*520_*521insACACACACACCCACAC MANE Select	NP_004773.1:n.*520_*521insACACACACACCCACAC