Canonical Allele Identifier: CA359245276
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716727A>G , CM000667.2:g.14716727A>G GRCh38
NC_000005.9:g.14716836A>G , CM000667.1:g.14716836A>G GRCh37
NC_000005.8:g.14769836A>G NCBI36
NG_008273.1:g.160052T>C
NG_008273.2:g.160059T>C
NG_051625.1:g.60934A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1120T>C MANE Select ENSP00000284268.6:p.Phe374Leu
ENST00000284268.6:c.1120T>C ENSP00000284268.6:p.Phe374Leu
ENST00000502585.1:n.362T>C
NM_054027.4:c.1120T>C NP_473368.1:p.Phe374Leu
NM_054027.5:c.1120T>C NP_473368.1:p.Phe374Leu
XM_017009644.2:c.1036T>C XP_016865133.1:p.Phe346Leu
NM_054027.6:c.1120T>C MANE Select NP_473368.1:p.Phe374Leu