Canonical Allele Identifier: CA1528949040

Gene: ANKH

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871348T= , CM000667.2:g.14871348T=	GRCh38
NC_000005.9:g.14871457T= , CM000667.1:g.14871457T=	GRCh37
NC_000005.8:g.14924457T=	NCBI36
NG_008273.1:g.5431A=
NG_008273.2:g.5438A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000284268.8:c.96+4A= MANE Select	ENSP00000284268.6:n.96+4A=
ENST00000284268.6:c.96+4A=	ENSP00000284268.6:n.96+4A=
ENST00000505140.1:c.100A=	ENSP00000426332.1:p.Ser34=
ENST00000513115.1:n.121+4A=
NM_054027.4:c.96+4A=	NP_473368.1:n.96+4A=
XM_011514067.1:c.96+4A=	XP_011512369.1:n.96+4A=
NM_054027.5:c.96+4A=	NP_473368.1:n.96+4A=
NM_054027.6:c.96+4A= MANE Select	NP_473368.1:n.96+4A=