Canonical Allele Identifier: CA7313798

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92005673T>C , CM000676.2:g.92005673T>C	GRCh38
NC_000014.8:g.92472017T>C , CM000676.1:g.92472017T>C	GRCh37
NC_000014.7:g.91541770T>C	NCBI36
NG_016970.1:g.39387A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.2303A>G MANE Select	NP_004230.2:p.Asn768Ser
ENST00000267622.8:c.2303A>G MANE Select	ENSP00000267622.4:p.Asn768Ser
NM_001321851.1:c.2300A>G	NP_001308780.1:p.Asn767Ser
NM_004239.3:c.2303A>G	NP_004230.2:p.Asn768Ser
ENST00000554357.5:c.1449A>G
XM_005268214.2:c.977A>G	XP_005268271.1:p.Asn326Ser
XM_005268215.2:c.1527+1967A>G	XP_005268272.1:n.1527+1967A>G
XM_006720321.2:c.2300A>G	XP_006720384.1:p.Asn767Ser
XM_011537361.1:c.2303A>G	XP_011535663.1:p.Asn768Ser
XM_017021787.2:c.1598A>G	XP_016877276.1:p.Asn533Ser
XM_017021788.2:c.977A>G	XP_016877277.1:p.Asn326Ser
XR_001750598.2:n.2752A>G
XR_943560.1:n.2758A>G
XR_943560.2:n.2752A>G