Canonical Allele Identifier: CA374947671

Gene: AK1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.867G>T
ENST00000643029.1:c.*2042G>T	ENSP00000496586.1:n.*2042G>T
ENST00000643338.1:c.*1931G>T	ENSP00000495890.1:n.*1931G>T
ENST00000644144.2:c.367G>T MANE Select	ENSP00000494600.1:p.Glu123Ter
ENST00000645007.1:c.*2291G>T	ENSP00000494773.1:n.*2291G>T
ENST00000646171.1:c.*400G>T	ENSP00000495484.1:n.*400G>T
ENST00000223836.10:c.415G>T	ENSP00000223836.10:p.Glu139Ter
ENST00000373156.5:c.367G>T	ENSP00000362249.1:p.Glu123Ter
ENST00000373176.5:c.367G>T	ENSP00000362271.1:p.Glu123Ter
ENST00000413016.5:c.189G>T
ENST00000550143.5:c.147G>T	ENSP00000449130.1:p.Leu49=
ENST00000550992.1:c.*387G>T	ENSP00000448741.1:n.*387G>T
NM_000476.2:c.367G>T	NP_000467.1:p.Glu123Ter
XM_005251786.2:c.415G>T	XP_005251843.1:p.Glu139Ter
XM_011518348.1:c.367G>T	XP_011516650.1:p.Glu123Ter
XM_011518349.1:c.187G>T	XP_011516651.1:p.Glu63Ter
NM_001318121.1:c.367G>T	NP_001305050.1:p.Glu123Ter
NM_001318122.1:c.415G>T	NP_001305051.1:p.Glu139Ter
XM_017014428.1:c.367G>T	XP_016869917.1:p.Glu123Ter
XM_024447439.1:c.346G>T	XP_024303207.1:p.Glu116Ter
XM_024447440.1:c.187G>T	XP_024303208.1:p.Glu63Ter
NM_001318122.2:c.415G>T	NP_001305051.1:p.Glu139Ter
NM_000476.3:c.367G>T MANE Select	NP_000467.1:p.Glu123Ter
NR_174625.1:n.3686G>T
NR_174626.1:n.3529G>T
NR_174627.1:n.3566G>T
NR_174628.1:n.2944G>T
NR_174629.1:n.2889G>T
NR_174630.1:n.2925G>T
NR_174631.1:n.2870G>T
NR_174632.1:n.2959G>T