Canonical Allele Identifier: CA2266662059

Gene: ANKFN1

Linked Data

• dbSNP Id: rs1906175939

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.56114966C>A , CM000679.2:g.56114966C>A	GRCh38
NC_000017.10:g.54192327C>A , CM000679.1:g.54192327C>A	GRCh37
NC_000017.9:g.51547326C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000635860.2:c.288+68641C>A	ENSP00000489811.2:n.288+68641C>A
ENST00000635860.1:c.288+68641C>A	ENSP00000489811.1:n.288+68641C>A
ENST00000653862.1:c.462+68641C>A	ENSP00000499705.1:n.462+68641C>A
ENST00000575594.1:n.89+3920C>A
XM_011524425.1:c.-78+3920C>A	XP_011522727.1:n.-78+3920C>A
XM_011524430.1:c.-261+3920C>A	XP_011522732.1:n.-261+3920C>A
XM_011524431.1:c.-193+3920C>A	XP_011522733.1:n.-193+3920C>A
XM_011524432.1:c.288+68641C>A	XP_011522734.1:n.288+68641C>A
XM_011524430.2:c.-261+3920C>A	XP_011522732.1:n.-261+3920C>A
XM_011524431.2:c.-193+3920C>A	XP_011522733.1:n.-193+3920C>A
XM_017024263.1:c.-78+3920C>A	XP_016879752.1:n.-78+3920C>A
XM_017024270.2:c.-78+3920C>A	XP_016879759.1:n.-78+3920C>A