Canonical Allele Identifier: CA265637724

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91975422T>C , CM000676.2:g.91975422T>C	GRCh38
NC_000014.8:g.92441766T>C , CM000676.1:g.92441766T>C	GRCh37
NC_000014.7:g.91511519T>C	NCBI36
NG_016970.1:g.69638A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_004239.4:c.5343-136A>G MANE Select	NP_004230.2:n.5343-136A>G
ENST00000267622.8:c.5343-136A>G MANE Select	ENSP00000267622.4:n.5343-136A>G
NM_001321851.1:c.5340-136A>G	NP_001308780.1:n.5340-136A>G
NM_004239.3:c.5343-136A>G	NP_004230.2:n.5343-136A>G
ENST00000554357.5:c.4489-136A>G
ENST00000557017.1:c.714-136A>G	ENSP00000451607.1:n.714-136A>G
XM_005268214.2:c.4017-136A>G	XP_005268271.1:n.4017-136A>G
XM_005268215.2:c.2313-136A>G	XP_005268272.1:n.2313-136A>G
XM_006720321.2:c.5340-136A>G	XP_006720384.1:n.5340-136A>G
XM_017021787.2:c.4638-136A>G	XP_016877276.1:n.4638-136A>G
XM_017021788.2:c.4017-136A>G	XP_016877277.1:n.4017-136A>G
XR_943560.1:n.5921-136A>G
XR_943560.2:n.5915-136A>G