Canonical Allele Identifier: CA359245290
Gene: ANKH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716734C>G , CM000667.2:g.14716734C>G GRCh38
NC_000005.9:g.14716843C>G , CM000667.1:g.14716843C>G GRCh37
NC_000005.8:g.14769843C>G NCBI36
NG_008273.1:g.160045G>C
NG_008273.2:g.160052G>C
NG_051625.1:g.60941C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1113G>C MANE Select ENSP00000284268.6:p.Leu371Phe
ENST00000284268.6:c.1113G>C ENSP00000284268.6:p.Leu371Phe
ENST00000502585.1:n.355G>C
NM_054027.4:c.1113G>C NP_473368.1:p.Leu371Phe
NM_054027.5:c.1113G>C NP_473368.1:p.Leu371Phe
XM_017009644.2:c.1029G>C XP_016865133.1:p.Leu343Phe
NM_054027.6:c.1113G>C MANE Select NP_473368.1:p.Leu371Phe