Canonical Allele Identifier: CA2510353389
Gene: TRAIP HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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