Canonical Allele Identifier: CA1363671497
Gene: TRAIP HGNC NCBI

Linked Data

dbSNP Id: rs2081705855

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.49828888T>C , CM000665.2:g.49828888T>C GRCh38
NC_000003.11:g.49866321T>C , CM000665.1:g.49866321T>C GRCh37
NC_000003.10:g.49841325T>C NCBI36
NG_046695.1:g.32672A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000331456.7:c.*215A>G MANE Select ENSP00000328203.2:n.*215A>G
ENST00000331456.6:c.*215A>G ENSP00000328203.2:n.*215A>G
ENST00000491060.1:n.779A>G
NM_005879.2:c.*215A>G NP_005870.2:n.*215A>G
XM_011533264.1:c.*215A>G XP_011531566.1:n.*215A>G
XM_017005526.1:c.*215A>G XP_016861015.1:n.*215A>G
XR_001739979.1:n.1829A>G
NM_005879.3:c.*215A>G MANE Select NP_005870.2:n.*215A>G