Canonical Allele Identifier: CA938948376

Gene: OVOL1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65793149C>A , CM000673.2:g.65793149C>A	GRCh38
NC_000011.9:g.65560620C>A , CM000673.1:g.65560620C>A	GRCh37
NC_000011.8:g.65317196C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000335987.8:c.101-882C>A MANE Select	ENSP00000337862.3:n.101-882C>A
ENST00000335987.7:c.101-882C>A	ENSP00000337862.3:n.101-882C>A
ENST00000531907.1:n.493+699C>A
NM_004561.3:c.101-882C>A	NP_004552.2:n.101-882C>A
XM_005274018.3:c.-86-882C>A	XP_005274075.1:n.-86-882C>A
XM_011545067.1:c.-86-882C>A	XP_011543369.1:n.-86-882C>A
XM_011545068.1:c.-86-882C>A	XP_011543370.1:n.-86-882C>A
XM_011545067.2:c.-86-882C>A	XP_011543369.1:n.-86-882C>A
XM_011545068.3:c.-86-882C>A	XP_011543370.1:n.-86-882C>A
XM_017017837.1:c.-86-882C>A	XP_016873326.1:n.-86-882C>A
XM_017017838.2:c.-87+699C>A	XP_016873327.1:n.-87+699C>A
NM_004561.4:c.101-882C>A MANE Select	NP_004552.2:n.101-882C>A