Canonical Allele Identifier: CA2844613142
Community Standard Title: NC_000017.11:g.56115162A>T
Gene: ANKFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56115162A>T , CM000679.2:g.56115162A>T GRCh38
NC_000017.10:g.54192523A>T , CM000679.1:g.54192523A>T GRCh37
NC_000017.9:g.51547522A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000575594.1:n.89+4116A>T
ENST00000635860.1:c.288+68837A>T ENSP00000489811.1:n.288+68837A>T
ENST00000635860.2:c.288+68837A>T ENSP00000489811.2:n.288+68837A>T
ENST00000653862.1:c.462+68837A>T ENSP00000499705.1:n.462+68837A>T
XM_011524425.1:c.-78+4116A>T XP_011522727.1:n.-78+4116A>T
XM_011524430.1:c.-261+4116A>T XP_011522732.1:n.-261+4116A>T
XM_011524430.2:c.-261+4116A>T XP_011522732.1:n.-261+4116A>T
XM_011524431.1:c.-193+4116A>T XP_011522733.1:n.-193+4116A>T
XM_011524431.2:c.-193+4116A>T XP_011522733.1:n.-193+4116A>T
XM_011524432.1:c.288+68837A>T XP_011522734.1:n.288+68837A>T
XM_017024263.1:c.-78+4116A>T XP_016879752.1:n.-78+4116A>T
XM_017024270.2:c.-78+4116A>T XP_016879759.1:n.-78+4116A>T