Canonical Allele Identifier: CA390651356

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92004157A>C , CM000676.2:g.92004157A>C	GRCh38
NC_000014.8:g.92470501A>C , CM000676.1:g.92470501A>C	GRCh37
NC_000014.7:g.91540254A>C	NCBI36
NG_016970.1:g.40903T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.3819T>G MANE Select	ENSP00000267622.4:p.Ser1273Arg
ENST00000554357.5:c.2965T>G
NM_004239.3:c.3819T>G	NP_004230.2:p.Ser1273Arg
XM_005268214.2:c.2493T>G	XP_005268271.1:p.Ser831Arg
XM_005268215.2:c.1527+3483T>G	XP_005268272.1:n.1527+3483T>G
XM_006720321.2:c.3816T>G	XP_006720384.1:p.Ser1272Arg
XM_011537361.1:c.3819T>G	XP_011535663.1:p.Ser1273Arg
XR_943560.1:n.4274T>G
NM_001321851.1:c.3816T>G	NP_001308780.1:p.Ser1272Arg
NM_004239.4:c.3819T>G MANE Select	NP_004230.2:p.Ser1273Arg
XM_017021787.2:c.3114T>G	XP_016877276.1:p.Ser1038Arg
XM_017021788.2:c.2493T>G	XP_016877277.1:p.Ser831Arg
XR_001750598.2:n.4268T>G
XR_943560.2:n.4268T>G