Canonical Allele Identifier: CA1528949227
Gene: ANKH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871588G= , CM000667.2:g.14871588G= GRCh38
NC_000005.9:g.14871697G= , CM000667.1:g.14871697G= GRCh37
NC_000005.8:g.14924697G= NCBI36
NG_008273.1:g.5191C=
NG_008273.2:g.5198C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-141C= MANE Select ENSP00000284268.6:n.-141C=
ENST00000284268.6:c.-141C= ENSP00000284268.6:n.-141C=
ENST00000505140.1:c.-141C= ENSP00000426332.1:n.-141C=
NM_054027.4:c.-141C= NP_473368.1:n.-141C=
XM_011514067.1:c.-141C= XP_011512369.1:n.-141C=
NM_054027.5:c.-141C= NP_473368.1:n.-141C=
NM_054027.6:c.-141C= MANE Select NP_473368.1:n.-141C=
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