Canonical Allele Identifier: CA2983110410
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14871339_14871340del , CM000667.2:g.14871339_14871340del GRCh38
NC_000005.9:g.14871448_14871449del , CM000667.1:g.14871448_14871449del GRCh37
NC_000005.8:g.14924448_14924449del NCBI36
NG_008273.1:g.5441_5442del
NG_008273.2:g.5448_5449del

Transcript Alleles

HGVS Amino-acid Change
ENST00000284268.8:c.96+14_96+15del MANE Select ENSP00000284268.6:n.96+14_96+15del
ENST00000284268.6:c.96+14_96+15del ENSP00000284268.6:n.96+14_96+15del
ENST00000505140.1:c.110_111del ENSP00000426332.1:p.Pro37ArgfsTer?
ENST00000513115.1:n.121+14_121+15del
NM_054027.4:c.96+14_96+15del NP_473368.1:n.96+14_96+15del
XM_011514067.1:c.96+14_96+15del XP_011512369.1:n.96+14_96+15del
NM_054027.5:c.96+14_96+15del NP_473368.1:n.96+14_96+15del
NM_054027.6:c.96+14_96+15del MANE Select NP_473368.1:n.96+14_96+15del