Canonical Allele Identifier: CA2180843988
Gene: FAM81A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.59419539_59419541delinsCTT , CM000677.2:g.59419539_59419541delinsCTT GRCh38
NC_000015.9:g.59711738_59711740delinsCTT , CM000677.1:g.59711738_59711740delinsCTT GRCh37
NC_000015.8:g.57499030_57499032delinsCTT NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000558348.5:c.-78+17181_-78+17183delinsCTT ENSP00000453918.1:n.-78+17181_-78+17183de...
ENST00000560394.5:c.-78+17181_-78+17183delinsCTT ENSP00000452962.1:n.-78+17181_-78+17183de...
XM_006720399.1:c.-78+17181_-78+17183delinsCTT XP_006720462.1:n.-78+17181_-78+17183delin...
XM_011521248.1:c.-22+17181_-22+17183delinsCTT XP_011519550.1:n.-22+17181_-22+17183delin...
XM_011521248.2:c.-22+17181_-22+17183delinsCTT XP_011519550.1:n.-22+17181_-22+17183delin...