Canonical Allele Identifier: CA1528949036
Gene: ANKH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871342C= , CM000667.2:g.14871342C= GRCh38
NC_000005.9:g.14871451C= , CM000667.1:g.14871451C= GRCh37
NC_000005.8:g.14924451C= NCBI36
NG_008273.1:g.5437G=
NG_008273.2:g.5444G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.96+10G= MANE Select ENSP00000284268.6:n.96+10G=
ENST00000284268.6:c.96+10G= ENSP00000284268.6:n.96+10G=
ENST00000505140.1:c.106G= ENSP00000426332.1:p.Gly36=
ENST00000513115.1:n.121+10G=
NM_054027.4:c.96+10G= NP_473368.1:n.96+10G=
XM_011514067.1:c.96+10G= XP_011512369.1:n.96+10G=
NM_054027.5:c.96+10G= NP_473368.1:n.96+10G=
NM_054027.6:c.96+10G= MANE Select NP_473368.1:n.96+10G=
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