Canonical Allele Identifier: CA359245268
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716724A>T , CM000667.2:g.14716724A>T GRCh38
NC_000005.9:g.14716833A>T , CM000667.1:g.14716833A>T GRCh37
NC_000005.8:g.14769833A>T NCBI36
NG_008273.1:g.160055T>A
NG_008273.2:g.160062T>A
NG_051625.1:g.60931A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1123T>A MANE Select ENSP00000284268.6:p.Ser375Thr
ENST00000284268.6:c.1123T>A ENSP00000284268.6:p.Ser375Thr
ENST00000502585.1:n.365T>A
NM_054027.4:c.1123T>A NP_473368.1:p.Ser375Thr
NM_054027.5:c.1123T>A NP_473368.1:p.Ser375Thr
XM_017009644.2:c.1039T>A XP_016865133.1:p.Ser347Thr
NM_054027.6:c.1123T>A MANE Select NP_473368.1:p.Ser375Thr