Canonical Allele Identifier: CA2266662027
Gene: ANKFN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56114907_56114908delinsAG , CM000679.2:g.56114907_56114908delinsAG GRCh38
NC_000017.10:g.54192268_54192269delinsAG , CM000679.1:g.54192268_54192269delinsAG GRCh37
NC_000017.9:g.51547267_51547268delinsAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000635860.2:c.288+68582_288+68583delinsAG ENSP00000489811.2:n.288+68582_288+68583delinsAG
ENST00000635860.1:c.288+68582_288+68583delinsAG ENSP00000489811.1:n.288+68582_288+68583delinsAG
ENST00000653862.1:c.462+68582_462+68583delinsAG ENSP00000499705.1:n.462+68582_462+68583delinsAG
ENST00000575594.1:n.89+3861_89+3862delinsAG
XM_011524425.1:c.-78+3861_-78+3862delinsAG XP_011522727.1:n.-78+3861_-78+3862delinsAG
XM_011524430.1:c.-261+3861_-261+3862delinsAG XP_011522732.1:n.-261+3861_-261+3862delinsAG
XM_011524431.1:c.-193+3861_-193+3862delinsAG XP_011522733.1:n.-193+3861_-193+3862delinsAG
XM_011524432.1:c.288+68582_288+68583delinsAG XP_011522734.1:n.288+68582_288+68583delinsAG
XM_011524430.2:c.-261+3861_-261+3862delinsAG XP_011522732.1:n.-261+3861_-261+3862delinsAG
XM_011524431.2:c.-193+3861_-193+3862delinsAG XP_011522733.1:n.-193+3861_-193+3862delinsAG
XM_017024263.1:c.-78+3861_-78+3862delinsAG XP_016879752.1:n.-78+3861_-78+3862delinsAG
XM_017024270.2:c.-78+3861_-78+3862delinsAG XP_016879759.1:n.-78+3861_-78+3862delinsAG