Canonical Allele Identifier: CA1979406085
Gene: OVOL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.65791837_65791839delinsCAG , CM000673.2:g.65791837_65791839delinsCAG GRCh38
NC_000011.9:g.65559308_65559310delinsCAG , CM000673.1:g.65559308_65559310delinsCAG GRCh37
NC_000011.8:g.65315884_65315886delinsCAG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000335987.8:c.101-2194_101-2192delinsCAG MANE Select ENSP00000337862.3:n.101-2194_101-2192deli...
ENST00000335987.7:c.101-2194_101-2192delinsCAG ENSP00000337862.3:n.101-2194_101-2192deli...
ENST00000531907.1:n.361-481_361-479delinsCAG
NM_004561.3:c.101-2194_101-2192delinsCAG NP_004552.2:n.101-2194_101-2192delinsCAG
XM_005274018.3:c.-87+2144_-87+2146delinsCAG XP_005274075.1:n.-87+2144_-87+2146delinsC...
XM_011545067.1:c.-86-2194_-86-2192delinsCAG XP_011543369.1:n.-86-2194_-86-2192delinsC...
XM_011545068.1:c.-87+974_-87+976delinsCAG XP_011543370.1:n.-87+974_-87+976delinsCAG...
XM_011545067.2:c.-86-2194_-86-2192delinsCAG XP_011543369.1:n.-86-2194_-86-2192delinsC...
XM_011545068.3:c.-87+974_-87+976delinsCAG XP_011543370.1:n.-87+974_-87+976delinsCAG...
XM_017017837.1:c.-86-2194_-86-2192delinsCAG XP_016873326.1:n.-86-2194_-86-2192delinsC...
NM_004561.4:c.101-2194_101-2192delinsCAG MANE Select NP_004552.2:n.101-2194_101-2192delinsCAG