Canonical Allele Identifier: CA487569867

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91976116T>C , CM000676.2:g.91976116T>C	GRCh38
NC_000014.8:g.92442460T>C , CM000676.1:g.92442460T>C	GRCh37
NC_000014.7:g.91512213T>C	NCBI36
NG_016970.1:g.68944A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.5334A>G MANE Select	NP_004230.2:p.Lys1778=
ENST00000267622.8:c.5334A>G MANE Select	ENSP00000267622.4:p.Lys1778=
NM_001321851.1:c.5331A>G	NP_001308780.1:p.Lys1777=
NM_004239.3:c.5334A>G	NP_004230.2:p.Lys1778=
ENST00000554357.5:c.4480A>G
ENST00000557017.1:c.705A>G	ENSP00000451607.1:n.705A>G
XM_005268214.2:c.4008A>G	XP_005268271.1:p.Lys1336=
XM_005268215.2:c.2304A>G	XP_005268272.1:p.Lys768=
XM_006720321.2:c.5331A>G	XP_006720384.1:p.Lys1777=
XM_017021787.2:c.4629A>G	XP_016877276.1:p.Lys1543=
XM_017021788.2:c.4008A>G	XP_016877277.1:p.Lys1336=
XR_943560.1:n.5912A>G
XR_943560.2:n.5906A>G