Canonical Allele Identifier: CA1528949272
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871647C= , CM000667.2:g.14871647C= GRCh38
NC_000005.9:g.14871756C= , CM000667.1:g.14871756C= GRCh37
NC_000005.8:g.14924756C= NCBI36
NG_008273.1:g.5132G=
NG_008273.2:g.5139G=

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.-200G= MANE Select ENSP00000284268.6:n.-200G=
ENST00000284268.6:c.-200G= ENSP00000284268.6:n.-200G=
ENST00000505140.1:c.-200G= ENSP00000426332.1:n.-200G=
NM_054027.4:c.-200G= NP_473368.1:n.-200G=
XM_011514067.1:c.-200G= XP_011512369.1:n.-200G=
NM_054027.5:c.-200G= NP_473368.1:n.-200G=
NM_054027.6:c.-200G= MANE Select NP_473368.1:n.-200G=