Canonical Allele Identifier: CA2738111800
Gene: SNAP29 HGNC NCBI

Linked Data

dbSNP Id: rs2147875234

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888350_20888354del , CM000684.2:g.20888350_20888354del GRCh38
NC_000022.10:g.21242638_21242642del , CM000684.1:g.21242638_21242642del GRCh37
NC_000022.9:g.19572638_19572642del NCBI36
NG_012152.1:g.34347_34351del

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*514_*518del MANE Select ENSP00000215730.6:n.*514_*518del
ENST00000215730.11:c.*514_*518del ENSP00000215730.6:n.*514_*518del
NM_004782.3:c.*514_*518del NP_004773.1:n.*514_*518del
NM_004782.4:c.*514_*518del MANE Select NP_004773.1:n.*514_*518del