Canonical Allele Identifier: CA359245282
Gene: ANKH HGNC NCBI

Linked Data

gnomAD v4: 5-14716730-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716730T>A , CM000667.2:g.14716730T>A GRCh38
NC_000005.9:g.14716839T>A , CM000667.1:g.14716839T>A GRCh37
NC_000005.8:g.14769839T>A NCBI36
NG_008273.1:g.160049A>T
NG_008273.2:g.160056A>T
NG_051625.1:g.60937T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1117A>T MANE Select ENSP00000284268.6:p.Ile373Phe
ENST00000284268.6:c.1117A>T ENSP00000284268.6:p.Ile373Phe
ENST00000502585.1:n.359A>T
NM_054027.4:c.1117A>T NP_473368.1:p.Ile373Phe
NM_054027.5:c.1117A>T NP_473368.1:p.Ile373Phe
XM_017009644.2:c.1033A>T XP_016865133.1:p.Ile345Phe
NM_054027.6:c.1117A>T MANE Select NP_473368.1:p.Ile373Phe