Canonical Allele Identifier: CA1528949175
Gene: ANKH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871536C= , CM000667.2:g.14871536C= GRCh38
NC_000005.9:g.14871645C= , CM000667.1:g.14871645C= GRCh37
NC_000005.8:g.14924645C= NCBI36
NG_008273.1:g.5243G=
NG_008273.2:g.5250G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.-89G= MANE Select ENSP00000284268.6:n.-89G=
ENST00000284268.6:c.-89G= ENSP00000284268.6:n.-89G=
ENST00000505140.1:c.-89G= ENSP00000426332.1:n.-89G=
NM_054027.4:c.-89G= NP_473368.1:n.-89G=
XM_011514067.1:c.-89G= XP_011512369.1:n.-89G=
NM_054027.5:c.-89G= NP_473368.1:n.-89G=
NM_054027.6:c.-89G= MANE Select NP_473368.1:n.-89G=
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