Canonical Allele Identifier: CA359285982

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14871462T>A (hg19) ; chr5:g.14871353T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14871353T>A , CM000667.2:g.14871353T>A	GRCh38
NC_000005.9:g.14871462T>A , CM000667.1:g.14871462T>A	GRCh37
NC_000005.8:g.14924462T>A	NCBI36
NG_008273.1:g.5426A>T
NG_008273.2:g.5433A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.95A>T MANE Select	ENSP00000284268.6:p.Gln32Leu
ENST00000284268.6:c.95A>T	ENSP00000284268.6:p.Gln32Leu
ENST00000505140.1:c.95A>T	ENSP00000426332.1:p.Gln32Leu
ENST00000513115.1:n.120A>T
NM_054027.4:c.95A>T	NP_473368.1:p.Gln32Leu
XM_011514067.1:c.95A>T	XP_011512369.1:p.Gln32Leu
NM_054027.5:c.95A>T	NP_473368.1:p.Gln32Leu
NM_054027.6:c.95A>T MANE Select	NP_473368.1:p.Gln32Leu