Canonical Allele Identifier: CA7313897

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92006387C>T , CM000676.2:g.92006387C>T	GRCh38
NC_000014.8:g.92472731C>T , CM000676.1:g.92472731C>T	GRCh37
NC_000014.7:g.91542484C>T	NCBI36
NG_016970.1:g.38673G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.1589G>A MANE Select	ENSP00000267622.4:p.Ser530Asn
ENST00000554357.5:c.735G>A
NM_004239.3:c.1589G>A	NP_004230.2:p.Ser530Asn
XM_005268214.2:c.263G>A	XP_005268271.1:p.Ser88Asn
XM_005268215.2:c.1527+1253G>A	XP_005268272.1:n.1527+1253G>A
XM_006720321.2:c.1586G>A	XP_006720384.1:p.Ser529Asn
XM_011537361.1:c.1589G>A	XP_011535663.1:p.Ser530Asn
XR_943560.1:n.2044G>A
NM_001321851.1:c.1586G>A	NP_001308780.1:p.Ser529Asn
NM_004239.4:c.1589G>A MANE Select	NP_004230.2:p.Ser530Asn
XM_017021787.2:c.884G>A	XP_016877276.1:p.Ser295Asn
XM_017021788.2:c.263G>A	XP_016877277.1:p.Ser88Asn
XR_001750598.2:n.2038G>A
XR_943560.2:n.2038G>A