Canonical Allele Identifier: CA1979406141

Gene: OVOL1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.65791890T= , CM000673.2:g.65791890T=	GRCh38
NC_000011.9:g.65559361T= , CM000673.1:g.65559361T=	GRCh37
NC_000011.8:g.65315937T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000335987.8:c.101-2141T= MANE Select	ENSP00000337862.3:n.101-2141T=
ENST00000335987.7:c.101-2141T=	ENSP00000337862.3:n.101-2141T=
ENST00000531907.1:n.361-428T=
NM_004561.3:c.101-2141T=	NP_004552.2:n.101-2141T=
XM_005274018.3:c.-86-2141T=	XP_005274075.1:n.-86-2141T=
XM_011545067.1:c.-86-2141T=	XP_011543369.1:n.-86-2141T=
XM_011545068.1:c.-87+1027T=	XP_011543370.1:n.-87+1027T=
XM_011545067.2:c.-86-2141T=	XP_011543369.1:n.-86-2141T=
XM_011545068.3:c.-87+1027T=	XP_011543370.1:n.-87+1027T=
XM_017017837.1:c.-86-2141T=	XP_016873326.1:n.-86-2141T=
NM_004561.4:c.101-2141T= MANE Select	NP_004552.2:n.101-2141T=