Canonical Allele Identifier: CA1528892440
Gene: ANKH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.14741837A= , CM000667.2:g.14741837A= GRCh38
NC_000005.9:g.14741946A= , CM000667.1:g.14741946A= GRCh37
NC_000005.8:g.14794946A= NCBI36
NG_008273.1:g.134942T=
NG_008273.2:g.134949T=

Transcript Alleles

HGVS Amino-acid change
ENST00000284268.8:c.1001T= MANE Select ENSP00000284268.6:p.Leu334=
ENST00000284268.6:c.1001T= ENSP00000284268.6:p.Leu334=
ENST00000503939.5:n.513T=
ENST00000515517.1:n.235T=
NM_054027.4:c.1001T= NP_473368.1:p.Leu334=
XM_011514067.1:c.1001T= XP_011512369.1:p.Leu334=
NM_054027.5:c.1001T= NP_473368.1:p.Leu334=
XM_017009644.2:c.917T= XP_016865133.1:p.Leu306=
NM_054027.6:c.1001T= MANE Select NP_473368.1:p.Leu334=