Canonical Allele Identifier: CA359245568

Gene: ANKH

Linked Data

• MyVariant Identifiers: chr5:g.14741955C>T (hg19) ; chr5:g.14741846C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14741846C>T , CM000667.2:g.14741846C>T	GRCh38
NC_000005.9:g.14741955C>T , CM000667.1:g.14741955C>T	GRCh37
NC_000005.8:g.14794955C>T	NCBI36
NG_008273.1:g.134933G>A
NG_008273.2:g.134940G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000284268.8:c.992G>A MANE Select	ENSP00000284268.6:p.Cys331Tyr
ENST00000284268.6:c.992G>A	ENSP00000284268.6:p.Cys331Tyr
ENST00000503939.5:n.504G>A
ENST00000515517.1:n.226G>A
NM_054027.4:c.992G>A	NP_473368.1:p.Cys331Tyr
XM_011514067.1:c.992G>A	XP_011512369.1:p.Cys331Tyr
NM_054027.5:c.992G>A	NP_473368.1:p.Cys331Tyr
XM_017009644.2:c.908G>A	XP_016865133.1:p.Cys303Tyr
NM_054027.6:c.992G>A MANE Select	NP_473368.1:p.Cys331Tyr