Canonical Allele Identifier: CA805330788

Gene: ANKH

Linked Data

• dbSNP Id: rs1310333186
• gnomAD v3: 5-14741742-A-G
• gnomAD v4: 5-14741742-A-G
• MyVariant Identifiers: chr5:g.14741851A>G (hg19) ; chr5:g.14741742A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.14741742A>G , CM000667.2:g.14741742A>G	GRCh38
NC_000005.9:g.14741851A>G , CM000667.1:g.14741851A>G	GRCh37
NC_000005.8:g.14794851A>G	NCBI36
NG_008273.1:g.135037T>C
NG_008273.2:g.135044T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000284268.8:c.1011+85T>C MANE Select	ENSP00000284268.6:n.1011+85T>C
ENST00000284268.6:c.1011+85T>C	ENSP00000284268.6:n.1011+85T>C
ENST00000503939.5:n.523+85T>C
ENST00000515517.1:n.330T>C
NM_054027.4:c.1011+85T>C	NP_473368.1:n.1011+85T>C
XM_011514067.1:c.1011+85T>C	XP_011512369.1:n.1011+85T>C
NM_054027.5:c.1011+85T>C	NP_473368.1:n.1011+85T>C
XM_017009644.2:c.927+85T>C	XP_016865133.1:n.927+85T>C
NM_054027.6:c.1011+85T>C MANE Select	NP_473368.1:n.1011+85T>C