Canonical Allele Identifier: CA359245283
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1117A>G MANE Select ENSP00000284268.6:p.Ile373Val
ENST00000284268.6:c.1117A>G ENSP00000284268.6:p.Ile373Val
ENST00000502585.1:n.359A>G
NM_054027.4:c.1117A>G NP_473368.1:p.Ile373Val
NM_054027.5:c.1117A>G NP_473368.1:p.Ile373Val
XM_017009644.2:c.1033A>G XP_016865133.1:p.Ile345Val
NM_054027.6:c.1117A>G MANE Select NP_473368.1:p.Ile373Val