Canonical Allele Identifier: CA374947661

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630746T>A (hg19) ; chr9:g.127868467T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868467T>A , CM000671.2:g.127868467T>A	GRCh38
NC_000009.11:g.130630746T>A , CM000671.1:g.130630746T>A	GRCh37
NC_000009.10:g.129670567T>A	NCBI36
NG_011792.1:g.14277A>T
NG_011792.2:g.14277A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000476274.7:n.870A>T
ENST00000643029.1:c.*2045A>T	ENSP00000496586.1:n.*2045A>T
ENST00000643338.1:c.*1934A>T	ENSP00000495890.1:n.*1934A>T
ENST00000644144.2:c.370A>T MANE Select	ENSP00000494600.1:p.Thr124Ser
ENST00000645007.1:c.*2294A>T	ENSP00000494773.1:n.*2294A>T
ENST00000646171.1:c.*403A>T	ENSP00000495484.1:n.*403A>T
ENST00000223836.10:c.418A>T	ENSP00000223836.10:p.Thr140Ser
ENST00000373156.5:c.370A>T	ENSP00000362249.1:p.Thr124Ser
ENST00000373176.5:c.370A>T	ENSP00000362271.1:p.Thr124Ser
ENST00000413016.5:c.192A>T
ENST00000550143.5:c.150A>T	ENSP00000449130.1:p.Arg50Ser
ENST00000550992.1:c.*390A>T	ENSP00000448741.1:n.*390A>T
NM_000476.2:c.370A>T	NP_000467.1:p.Thr124Ser
XM_005251786.2:c.418A>T	XP_005251843.1:p.Thr140Ser
XM_011518348.1:c.370A>T	XP_011516650.1:p.Thr124Ser
XM_011518349.1:c.190A>T	XP_011516651.1:p.Thr64Ser
NM_001318121.1:c.370A>T	NP_001305050.1:p.Thr124Ser
NM_001318122.1:c.418A>T	NP_001305051.1:p.Thr140Ser
XM_017014428.1:c.370A>T	XP_016869917.1:p.Thr124Ser
XM_024447439.1:c.349A>T	XP_024303207.1:p.Thr117Ser
XM_024447440.1:c.190A>T	XP_024303208.1:p.Thr64Ser
NM_001318122.2:c.418A>T	NP_001305051.1:p.Thr140Ser
NM_000476.3:c.370A>T MANE Select	NP_000467.1:p.Thr124Ser
NR_174625.1:n.3689A>T
NR_174626.1:n.3532A>T
NR_174627.1:n.3569A>T
NR_174628.1:n.2947A>T
NR_174629.1:n.2892A>T
NR_174630.1:n.2928A>T
NR_174631.1:n.2873A>T
NR_174632.1:n.2962A>T