Canonical Allele Identifier: CA390644795

Gene: TRIP11

Linked Data

• MyVariant Identifiers: chr14:g.92442496C>G (hg19) ; chr14:g.91976152C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.91976152C>G , CM000676.2:g.91976152C>G	GRCh38
NC_000014.8:g.92442496C>G , CM000676.1:g.92442496C>G	GRCh37
NC_000014.7:g.91512249C>G	NCBI36
NG_016970.1:g.68908G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.5298G>C MANE Select	ENSP00000267622.4:p.Lys1766Asn
ENST00000554357.5:c.4444G>C
ENST00000557017.1:c.669G>C	ENSP00000451607.1:n.669G>C
NM_004239.3:c.5298G>C	NP_004230.2:p.Lys1766Asn
XM_005268214.2:c.3972G>C	XP_005268271.1:p.Lys1324Asn
XM_005268215.2:c.2268G>C	XP_005268272.1:p.Lys756Asn
XM_006720321.2:c.5295G>C	XP_006720384.1:p.Lys1765Asn
XR_943560.1:n.5876G>C
NM_001321851.1:c.5295G>C	NP_001308780.1:p.Lys1765Asn
NM_004239.4:c.5298G>C MANE Select	NP_004230.2:p.Lys1766Asn
XM_017021787.2:c.4593G>C	XP_016877276.1:p.Lys1531Asn
XM_017021788.2:c.3972G>C	XP_016877277.1:p.Lys1324Asn
XR_943560.2:n.5870G>C