Canonical Allele Identifier: CA7313924

Gene: TRIP11

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.92007634T>C , CM000676.2:g.92007634T>C	GRCh38
NC_000014.8:g.92473978T>C , CM000676.1:g.92473978T>C	GRCh37
NC_000014.7:g.91543731T>C	NCBI36
NG_016970.1:g.37426A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267622.8:c.1527+6A>G MANE Select	ENSP00000267622.4:n.1527+6A>G
ENST00000554357.5:c.673+6A>G
NM_004239.3:c.1527+6A>G	NP_004230.2:n.1527+6A>G
XM_005268214.2:c.201+6A>G	XP_005268271.1:n.201+6A>G
XM_005268215.2:c.1527+6A>G	XP_005268272.1:n.1527+6A>G
XM_006720321.2:c.1524+6A>G	XP_006720384.1:n.1524+6A>G
XM_011537361.1:c.1527+6A>G	XP_011535663.1:n.1527+6A>G
XR_943560.1:n.1982+6A>G
NM_001321851.1:c.1524+6A>G	NP_001308780.1:n.1524+6A>G
NM_004239.4:c.1527+6A>G MANE Select	NP_004230.2:n.1527+6A>G
XM_017021787.2:c.822+6A>G	XP_016877276.1:n.822+6A>G
XM_017021788.2:c.201+6A>G	XP_016877277.1:n.201+6A>G
XR_001750598.2:n.1976+6A>G
XR_943560.2:n.1976+6A>G