Canonical Allele Identifier: CA2396589660
Gene: SNAP29 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888390T= , CM000684.2:g.20888390T= GRCh38
NC_000022.10:g.21242678T= , CM000684.1:g.21242678T= GRCh37
NC_000022.9:g.19572678T= NCBI36
NG_012152.1:g.34387T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*554T= MANE Select ENSP00000215730.6:n.*554T=
ENST00000215730.11:c.*554T= ENSP00000215730.6:n.*554T=
NM_004782.3:c.*554T= NP_004773.1:n.*554T=
NM_004782.4:c.*554T= MANE Select NP_004773.1:n.*554T=