Canonical Allele Identifier: CA1528880697
Gene: ANKH HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14716562T= , CM000667.2:g.14716562T= GRCh38
NC_000005.9:g.14716671T= , CM000667.1:g.14716671T= GRCh37
NC_000005.8:g.14769671T= NCBI36
NG_008273.1:g.160217A=
NG_008273.2:g.160224A=
NG_051625.1:g.60769T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.1141+144A= MANE Select ENSP00000284268.6:n.1141+144A=
ENST00000284268.6:c.1141+144A= ENSP00000284268.6:n.1141+144A=
ENST00000502585.1:n.383+144A=
NM_054027.4:c.1141+144A= NP_473368.1:n.1141+144A=
NM_054027.5:c.1141+144A= NP_473368.1:n.1141+144A=
XM_017009644.2:c.1057+144A= XP_016865133.1:n.1057+144A=
NM_054027.6:c.1141+144A= MANE Select NP_473368.1:n.1141+144A=
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