Canonical Allele Identifier: CA1979406052
Gene: OVOL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791812C= , CM000673.2:g.65791812C= GRCh38
NC_000011.9:g.65559283C= , CM000673.1:g.65559283C= GRCh37
NC_000011.8:g.65315859C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2219C= MANE Select ENSP00000337862.3:n.101-2219C=
ENST00000335987.7:c.101-2219C= ENSP00000337862.3:n.101-2219C=
ENST00000531907.1:n.361-506C=
NM_004561.3:c.101-2219C= NP_004552.2:n.101-2219C=
XM_005274018.3:c.-87+2119C= XP_005274075.1:n.-87+2119C=
XM_011545067.1:c.-86-2219C= XP_011543369.1:n.-86-2219C=
XM_011545068.1:c.-87+949C= XP_011543370.1:n.-87+949C=
XM_011545067.2:c.-86-2219C= XP_011543369.1:n.-86-2219C=
XM_011545068.3:c.-87+949C= XP_011543370.1:n.-87+949C=
XM_017017837.1:c.-86-2219C= XP_016873326.1:n.-86-2219C=
NM_004561.4:c.101-2219C= MANE Select NP_004552.2:n.101-2219C=