Canonical Allele Identifier: CA2396589621

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888349_20888352delinsACAC , CM000684.2:g.20888349_20888352delinsACAC	GRCh38
NC_000022.10:g.21242637_21242640delinsACAC , CM000684.1:g.21242637_21242640delinsACAC	GRCh37
NC_000022.9:g.19572637_19572640delinsACAC	NCBI36
NG_012152.1:g.34346_34349delinsACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*513_*516delinsACAC MANE Select	ENSP00000215730.6:n.*513_*516delinsACAC
ENST00000215730.11:c.*513_*516delinsACAC	ENSP00000215730.6:n.*513_*516delinsACAC
NM_004782.3:c.*513_*516delinsACAC	NP_004773.1:n.*513_*516delinsACAC
NM_004782.4:c.*513_*516delinsACAC MANE Select	NP_004773.1:n.*513_*516delinsACAC