Canonical Allele Identifier: CA15228616
Gene: TRAIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49840831C>G , CM000665.2:g.49840831C>G GRCh38
NC_000003.11:g.49878264C>G , CM000665.1:g.49878264C>G GRCh37
NC_000003.10:g.49853268C>G NCBI36
NG_046695.1:g.20729G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000331456.7:c.705+154G>C MANE Select ENSP00000328203.2:n.705+154G>C
ENST00000331456.6:c.705+154G>C ENSP00000328203.2:n.705+154G>C
ENST00000469027.5:c.241-458G>C ENSP00000420085.1:n.241-458G>C
ENST00000473195.5:c.281-458G>C ENSP00000419556.1:n.281-458G>C
ENST00000482582.5:c.657+154G>C ENSP00000418544.1:n.657+154G>C
NM_005879.2:c.705+154G>C NP_005870.2:n.705+154G>C
XM_011533264.1:c.474+154G>C XP_011531566.1:n.474+154G>C
XR_940361.1:n.815+154G>C
XM_017005526.1:c.409-458G>C XP_016861015.1:n.409-458G>C
XR_001739979.1:n.815+154G>C
NM_005879.3:c.705+154G>C MANE Select NP_005870.2:n.705+154G>C