Canonical Allele Identifier: CA751562915

Gene: SNAP29

Linked Data

• MyVariant Identifiers: chr22:g.21242644_21242645insCT (hg19) ; chr22:g.20888356_20888357insCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888356_20888357insCT , CM000684.2:g.20888356_20888357insCT	GRCh38
NC_000022.10:g.21242644_21242645insCT , CM000684.1:g.21242644_21242645insCT	GRCh37
NC_000022.9:g.19572644_19572645insCT	NCBI36
NG_012152.1:g.34353_34354insCT

Transcript Alleles

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