Canonical Allele Identifier: CA359245264
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716723G>A , CM000667.2:g.14716723G>A GRCh38
NC_000005.9:g.14716832G>A , CM000667.1:g.14716832G>A GRCh37
NC_000005.8:g.14769832G>A NCBI36
NG_008273.1:g.160056C>T
NG_008273.2:g.160063C>T
NG_051625.1:g.60930G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1124C>T MANE Select ENSP00000284268.6:p.Ser375Phe
ENST00000284268.6:c.1124C>T ENSP00000284268.6:p.Ser375Phe
ENST00000502585.1:n.366C>T
NM_054027.4:c.1124C>T NP_473368.1:p.Ser375Phe
NM_054027.5:c.1124C>T NP_473368.1:p.Ser375Phe
XM_017009644.2:c.1040C>T XP_016865133.1:p.Ser347Phe
NM_054027.6:c.1124C>T MANE Select NP_473368.1:p.Ser375Phe