Canonical Allele Identifier: CA2665773782
Gene: TRAIP HGNC NCBI

Linked Data

gnomAD v4: 3-49828977-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828977G>T , CM000665.2:g.49828977G>T GRCh38
NC_000003.11:g.49866410G>T , CM000665.1:g.49866410G>T GRCh37
NC_000003.10:g.49841414G>T NCBI36
NG_046695.1:g.32583C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.*126C>A MANE Select ENSP00000328203.2:n.*126C>A
ENST00000331456.6:c.*126C>A ENSP00000328203.2:n.*126C>A
ENST00000491060.1:n.690C>A
NM_005879.2:c.*126C>A NP_005870.2:n.*126C>A
XM_011533264.1:c.*126C>A XP_011531566.1:n.*126C>A
XM_017005526.1:c.*126C>A XP_016861015.1:n.*126C>A
XR_001739979.1:n.1740C>A
NM_005879.3:c.*126C>A MANE Select NP_005870.2:n.*126C>A