Canonical Allele Identifier: CA2396589602

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888339_20888357delinsACACACACACACACACACT , CM000684.2:g.20888339_20888357delinsACACACACACACACACACT	GRCh38
NC_000022.10:g.21242627_21242645delinsACACACACACACACACACT , CM000684.1:g.21242627_21242645delinsACACACACACACACACACT	GRCh37
NC_000022.9:g.19572627_19572645delinsACACACACACACACACACT	NCBI36
NG_012152.1:g.34336_34354delinsACACACACACACACACACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*503_*521delinsACACACACACACACACACT MANE Select	ENSP00000215730.6:n.*503_*521delinsACACACACACACACACACT
ENST00000215730.11:c.*503_*521delinsACACACACACACACACACT	ENSP00000215730.6:n.*503_*521delinsACACACACACACACACACT
NM_004782.3:c.*503_*521delinsACACACACACACACACACT	NP_004773.1:n.*503_*521delinsACACACACACACACACACT
NM_004782.4:c.*503_*521delinsACACACACACACACACACT MANE Select	NP_004773.1:n.*503_*521delinsACACACACACACACACACT