Canonical Allele Identifier: CA1979405982
Gene: OVOL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791758C= , CM000673.2:g.65791758C= GRCh38
NC_000011.9:g.65559229C= , CM000673.1:g.65559229C= GRCh37
NC_000011.8:g.65315805C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000335987.8:c.101-2273C= MANE Select ENSP00000337862.3:n.101-2273C=
ENST00000335987.7:c.101-2273C= ENSP00000337862.3:n.101-2273C=
ENST00000531907.1:n.361-560C=
NM_004561.3:c.101-2273C= NP_004552.2:n.101-2273C=
XM_005274018.3:c.-87+2065C= XP_005274075.1:n.-87+2065C=
XM_011545067.1:c.-86-2273C= XP_011543369.1:n.-86-2273C=
XM_011545068.1:c.-87+895C= XP_011543370.1:n.-87+895C=
XM_011545067.2:c.-86-2273C= XP_011543369.1:n.-86-2273C=
XM_011545068.3:c.-87+895C= XP_011543370.1:n.-87+895C=
XM_017017837.1:c.-86-2273C= XP_016873326.1:n.-86-2273C=
NM_004561.4:c.101-2273C= MANE Select NP_004552.2:n.101-2273C=