Canonical Allele Identifier: CA443289834

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14769283A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14769174A>T , CM000667.2:g.14769174A>T	GRCh38
NC_000005.9:g.14769283A>T , CM000667.1:g.14769283A>T	GRCh37
NC_000005.8:g.14822283A>T	NCBI36
NG_008273.1:g.107605T>A
NG_008273.2:g.107612T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000284268.8:c.114T>A MANE Select	ENSP00000284268.6:p.Ile38=
ENST00000284268.6:c.114T>A	ENSP00000284268.6:p.Ile38=
ENST00000503389.1:n.120T>A
ENST00000513115.1:n.139T>A
NM_054027.4:c.114T>A	NP_473368.1:p.Ile38=
XM_011514067.1:c.114T>A	XP_011512369.1:p.Ile38=
NM_054027.5:c.114T>A	NP_473368.1:p.Ile38=
XM_017009644.2:c.30T>A	XP_016865133.1:p.Ile10=
NM_054027.6:c.114T>A MANE Select	NP_473368.1:p.Ile38=