Canonical Allele Identifier: CA2568337754
Gene: ANKFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56115217_56115218insCACTAAAA , CM000679.2:g.56115217_56115218insCACTAAAA GRCh38
NC_000017.10:g.54192578_54192579insCACTAAAA , CM000679.1:g.54192578_54192579insCACTAAAA GRCh37
NC_000017.9:g.51547577_51547578insCACTAAAA NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000635860.2:c.288+68892_288+68893insCACTAAAA ENSP00000489811.2:n.288+68892_288+68893insCACTAAAA
ENST00000635860.1:c.288+68892_288+68893insCACTAAAA ENSP00000489811.1:n.288+68892_288+68893insCACTAAAA
ENST00000653862.1:c.462+68892_462+68893insCACTAAAA ENSP00000499705.1:n.462+68892_462+68893insCACTAAAA
ENST00000575594.1:n.89+4171_89+4172insCACTAAAA
XM_011524425.1:c.-78+4171_-78+4172insCACTAAAA XP_011522727.1:n.-78+4171_-78+4172insCACTAAAA
XM_011524430.1:c.-261+4171_-261+4172insCACTAAAA XP_011522732.1:n.-261+4171_-261+4172insCACTAAAA
XM_011524431.1:c.-193+4171_-193+4172insCACTAAAA XP_011522733.1:n.-193+4171_-193+4172insCACTAAAA
XM_011524432.1:c.288+68892_288+68893insCACTAAAA XP_011522734.1:n.288+68892_288+68893insCACTAAAA
XM_011524430.2:c.-261+4171_-261+4172insCACTAAAA XP_011522732.1:n.-261+4171_-261+4172insCACTAAAA
XM_011524431.2:c.-193+4171_-193+4172insCACTAAAA XP_011522733.1:n.-193+4171_-193+4172insCACTAAAA
XM_017024263.1:c.-78+4171_-78+4172insCACTAAAA XP_016879752.1:n.-78+4171_-78+4172insCACTAAAA
XM_017024270.2:c.-78+4171_-78+4172insCACTAAAA XP_016879759.1:n.-78+4171_-78+4172insCACTAAAA