Canonical Allele Identifier: CA7314131

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92017673T>G , CM000676.2:g.92017673T>G	GRCh38
NC_000014.8:g.92484017T>G , CM000676.1:g.92484017T>G	GRCh37
NC_000014.7:g.91553770T>G	NCBI36
NG_016970.1:g.27387A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.657+9A>C MANE Select	NP_004230.2:n.657+9A>C
ENST00000267622.8:c.657+9A>C MANE Select	ENSP00000267622.4:n.657+9A>C
NM_001321851.1:c.654+9A>C	NP_001308780.1:n.654+9A>C
NM_004239.3:c.657+9A>C	NP_004230.2:n.657+9A>C
ENST00000555516.6:c.174+9A>C	ENSP00000451944.1:n.174+9A>C
XM_005268215.2:c.657+9A>C	XP_005268272.1:n.657+9A>C
XM_006720321.2:c.654+9A>C	XP_006720384.1:n.654+9A>C
XM_011537361.1:c.657+9A>C	XP_011535663.1:n.657+9A>C
XM_017021787.2:c.-90+9A>C	XP_016877276.1:n.-90+9A>C
XM_017021788.2:c.-542+9A>C	XP_016877277.1:n.-542+9A>C
XR_001750598.2:n.1106+9A>C
XR_943560.1:n.1112+9A>C
XR_943560.2:n.1106+9A>C