Canonical Allele Identifier: CA374947114

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630662T>A (hg19) ; chr9:g.127868383T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868383T>A , CM000671.2:g.127868383T>A	GRCh38
NC_000009.11:g.130630662T>A , CM000671.1:g.130630662T>A	GRCh37
NC_000009.10:g.129670483T>A	NCBI36
NG_011792.1:g.14361A>T
NG_011792.2:g.14361A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.954A>T
ENST00000643029.1:c.*2129A>T	ENSP00000496586.1:n.*2129A>T
ENST00000643338.1:c.*2018A>T	ENSP00000495890.1:n.*2018A>T
ENST00000644144.2:c.454A>T MANE Select	ENSP00000494600.1:p.Thr152Ser
ENST00000645007.1:c.*2378A>T	ENSP00000494773.1:n.*2378A>T
ENST00000646171.1:c.*487A>T	ENSP00000495484.1:n.*487A>T
ENST00000223836.10:c.502A>T	ENSP00000223836.10:p.Thr168Ser
ENST00000373156.5:c.454A>T	ENSP00000362249.1:p.Thr152Ser
ENST00000373176.5:c.454A>T	ENSP00000362271.1:p.Thr152Ser
ENST00000413016.5:c.276A>T
ENST00000550143.5:c.234A>T	ENSP00000449130.1:n.234A>T
NM_000476.2:c.454A>T	NP_000467.1:p.Thr152Ser
XM_005251786.2:c.502A>T	XP_005251843.1:p.Thr168Ser
XM_011518348.1:c.454A>T	XP_011516650.1:p.Thr152Ser
XM_011518349.1:c.274A>T	XP_011516651.1:p.Thr92Ser
NM_001318121.1:c.454A>T	NP_001305050.1:p.Thr152Ser
NM_001318122.1:c.502A>T	NP_001305051.1:p.Thr168Ser
XM_017014428.1:c.454A>T	XP_016869917.1:p.Thr152Ser
XM_024447439.1:c.433A>T	XP_024303207.1:p.Thr145Ser
XM_024447440.1:c.274A>T	XP_024303208.1:p.Thr92Ser
NM_001318122.2:c.502A>T	NP_001305051.1:p.Thr168Ser
NM_000476.3:c.454A>T MANE Select	NP_000467.1:p.Thr152Ser
NR_174625.1:n.3773A>T
NR_174626.1:n.3616A>T
NR_174627.1:n.3653A>T
NR_174628.1:n.3031A>T
NR_174629.1:n.2976A>T
NR_174630.1:n.3012A>T
NR_174631.1:n.2957A>T
NR_174632.1:n.3046A>T