Canonical Allele Identifier: CA359245270
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716725G>C , CM000667.2:g.14716725G>C GRCh38
NC_000005.9:g.14716834G>C , CM000667.1:g.14716834G>C GRCh37
NC_000005.8:g.14769834G>C NCBI36
NG_008273.1:g.160054C>G
NG_008273.2:g.160061C>G
NG_051625.1:g.60932G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1122C>G MANE Select ENSP00000284268.6:p.Phe374Leu
ENST00000284268.6:c.1122C>G ENSP00000284268.6:p.Phe374Leu
ENST00000502585.1:n.364C>G
NM_054027.4:c.1122C>G NP_473368.1:p.Phe374Leu
NM_054027.5:c.1122C>G NP_473368.1:p.Phe374Leu
XM_017009644.2:c.1038C>G XP_016865133.1:p.Phe346Leu
NM_054027.6:c.1122C>G MANE Select NP_473368.1:p.Phe374Leu