Canonical Allele Identifier: CA2508300973
Gene: SNAP29 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.20888067_20888068insC , CM000684.2:g.20888067_20888068insC GRCh38
NC_000022.10:g.21242355_21242356insC , CM000684.1:g.21242355_21242356insC GRCh37
NC_000022.9:g.19572355_19572356insC NCBI36
NG_012152.1:g.34064_34065insC

Transcript Alleles

HGVS Amino-acid Change
ENST00000215730.12:c.*231_*232insC MANE Select ENSP00000215730.6:n.*231_*232insC
ENST00000215730.11:c.*231_*232insC ENSP00000215730.6:n.*231_*232insC
NM_004782.3:c.*231_*232insC NP_004773.1:n.*231_*232insC
NM_004782.4:c.*231_*232insC MANE Select NP_004773.1:n.*231_*232insC