Canonical Allele Identifier: CA74578353
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs892281686
MyVariant Identifiers: chr3:g.49866224G>A (hg19) chr3:g.49828791G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828791G>A , CM000665.2:g.49828791G>A GRCh38
NC_000003.11:g.49866224G>A , CM000665.1:g.49866224G>A GRCh37
NC_000003.10:g.49841228G>A NCBI36
NG_046695.1:g.32769C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*312C>T MANE Select ENSP00000328203.2:n.*312C>T
ENST00000331456.6:c.*312C>T ENSP00000328203.2:n.*312C>T
ENST00000491060.1:n.876C>T
NM_005879.2:c.*312C>T NP_005870.2:n.*312C>T
XM_011533264.1:c.*312C>T XP_011531566.1:n.*312C>T
XM_017005526.1:c.*312C>T XP_016861015.1:n.*312C>T
XR_001739979.1:n.1926C>T
NM_005879.3:c.*312C>T MANE Select NP_005870.2:n.*312C>T
Search 100 bp 5'
Search 100 bp 3'