Canonical Allele Identifier: CA374947672

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630749C>T (hg19) ; chr9:g.127868470C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868470C>T , CM000671.2:g.127868470C>T	GRCh38
NC_000009.11:g.130630749C>T , CM000671.1:g.130630749C>T	GRCh37
NC_000009.10:g.129670570C>T	NCBI36
NG_011792.1:g.14274G>A
NG_011792.2:g.14274G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.867G>A
ENST00000643029.1:c.*2042G>A	ENSP00000496586.1:n.*2042G>A
ENST00000643338.1:c.*1931G>A	ENSP00000495890.1:n.*1931G>A
ENST00000644144.2:c.367G>A MANE Select	ENSP00000494600.1:p.Glu123Lys
ENST00000645007.1:c.*2291G>A	ENSP00000494773.1:n.*2291G>A
ENST00000646171.1:c.*400G>A	ENSP00000495484.1:n.*400G>A
ENST00000223836.10:c.415G>A	ENSP00000223836.10:p.Glu139Lys
ENST00000373156.5:c.367G>A	ENSP00000362249.1:p.Glu123Lys
ENST00000373176.5:c.367G>A	ENSP00000362271.1:p.Glu123Lys
ENST00000413016.5:c.189G>A
ENST00000550143.5:c.147G>A	ENSP00000449130.1:p.Leu49=
ENST00000550992.1:c.*387G>A	ENSP00000448741.1:n.*387G>A
NM_000476.2:c.367G>A	NP_000467.1:p.Glu123Lys
XM_005251786.2:c.415G>A	XP_005251843.1:p.Glu139Lys
XM_011518348.1:c.367G>A	XP_011516650.1:p.Glu123Lys
XM_011518349.1:c.187G>A	XP_011516651.1:p.Glu63Lys
NM_001318121.1:c.367G>A	NP_001305050.1:p.Glu123Lys
NM_001318122.1:c.415G>A	NP_001305051.1:p.Glu139Lys
XM_017014428.1:c.367G>A	XP_016869917.1:p.Glu123Lys
XM_024447439.1:c.346G>A	XP_024303207.1:p.Glu116Lys
XM_024447440.1:c.187G>A	XP_024303208.1:p.Glu63Lys
NM_001318122.2:c.415G>A	NP_001305051.1:p.Glu139Lys
NM_000476.3:c.367G>A MANE Select	NP_000467.1:p.Glu123Lys
NR_174625.1:n.3686G>A
NR_174626.1:n.3529G>A
NR_174627.1:n.3566G>A
NR_174628.1:n.2944G>A
NR_174629.1:n.2889G>A
NR_174630.1:n.2925G>A
NR_174631.1:n.2870G>A
NR_174632.1:n.2959G>A