Canonical Allele Identifier: CA467223412

Gene: AK1

Linked Data

• dbSNP Id: rs1356518002
• gnomAD v2: 9-130630630-G-A
• gnomAD v4: 9-127868351-G-A
• MyVariant Identifiers: chr9:g.130630630G>A (hg19) ; chr9:g.127868351G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868351G>A , CM000671.2:g.127868351G>A	GRCh38
NC_000009.11:g.130630630G>A , CM000671.1:g.130630630G>A	GRCh37
NC_000009.10:g.129670451G>A	NCBI36
NG_011792.1:g.14393C>T
NG_011792.2:g.14393C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000476274.7:n.986C>T
ENST00000643029.1:c.*2161C>T	ENSP00000496586.1:n.*2161C>T
ENST00000643338.1:c.*2050C>T	ENSP00000495890.1:n.*2050C>T
ENST00000644144.2:c.486C>T MANE Select	ENSP00000494600.1:p.Ala162=
ENST00000645007.1:c.*2410C>T	ENSP00000494773.1:n.*2410C>T
ENST00000646171.1:c.*519C>T	ENSP00000495484.1:n.*519C>T
ENST00000223836.10:c.534C>T	ENSP00000223836.10:p.Ala178=
ENST00000373156.5:c.486C>T	ENSP00000362249.1:p.Ala162=
ENST00000373176.5:c.486C>T	ENSP00000362271.1:p.Ala162=
ENST00000413016.5:c.308C>T
ENST00000550143.5:c.266C>T	ENSP00000449130.1:n.266C>T
NM_000476.2:c.486C>T	NP_000467.1:p.Ala162=
XM_005251786.2:c.534C>T	XP_005251843.1:p.Ala178=
XM_011518348.1:c.486C>T	XP_011516650.1:p.Ala162=
XM_011518349.1:c.306C>T	XP_011516651.1:p.Ala102=
NM_001318121.1:c.486C>T	NP_001305050.1:p.Ala162=
NM_001318122.1:c.534C>T	NP_001305051.1:p.Ala178=
XM_017014428.1:c.486C>T	XP_016869917.1:p.Ala162=
XM_024447439.1:c.465C>T	XP_024303207.1:p.Ala155=
XM_024447440.1:c.306C>T	XP_024303208.1:p.Ala102=
NM_001318122.2:c.534C>T	NP_001305051.1:p.Ala178=
NM_000476.3:c.486C>T MANE Select	NP_000467.1:p.Ala162=
NR_174625.1:n.3805C>T
NR_174626.1:n.3648C>T
NR_174627.1:n.3685C>T
NR_174628.1:n.3063C>T
NR_174629.1:n.3008C>T
NR_174630.1:n.3044C>T
NR_174631.1:n.2989C>T
NR_174632.1:n.3078C>T