Canonical Allele Identifier: CA2396589554

Gene: SNAP29

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.20888306_20888310delinsATCAT , CM000684.2:g.20888306_20888310delinsATCAT	GRCh38
NC_000022.10:g.21242594_21242598delinsATCAT , CM000684.1:g.21242594_21242598delinsATCAT	GRCh37
NC_000022.9:g.19572594_19572598delinsATCAT	NCBI36
NG_012152.1:g.34303_34307delinsATCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000215730.12:c.*470_*474delinsATCAT MANE Select	ENSP00000215730.6:n.*470_*474delinsATCAT
ENST00000215730.11:c.*470_*474delinsATCAT	ENSP00000215730.6:n.*470_*474delinsATCAT
NM_004782.3:c.*470_*474delinsATCAT	NP_004773.1:n.*470_*474delinsATCAT
NM_004782.4:c.*470_*474delinsATCAT MANE Select	NP_004773.1:n.*470_*474delinsATCAT