Canonical Allele Identifier: CA374947658

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630745G>A (hg19) ; chr9:g.127868466G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868466G>A , CM000671.2:g.127868466G>A	GRCh38
NC_000009.11:g.130630745G>A , CM000671.1:g.130630745G>A	GRCh37
NC_000009.10:g.129670566G>A	NCBI36
NG_011792.1:g.14278C>T
NG_011792.2:g.14278C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000476274.7:n.871C>T
ENST00000643029.1:c.*2046C>T	ENSP00000496586.1:n.*2046C>T
ENST00000643338.1:c.*1935C>T	ENSP00000495890.1:n.*1935C>T
ENST00000644144.2:c.371C>T MANE Select	ENSP00000494600.1:p.Thr124Ile
ENST00000645007.1:c.*2295C>T	ENSP00000494773.1:n.*2295C>T
ENST00000646171.1:c.*404C>T	ENSP00000495484.1:n.*404C>T
ENST00000223836.10:c.419C>T	ENSP00000223836.10:p.Thr140Ile
ENST00000373156.5:c.371C>T	ENSP00000362249.1:p.Thr124Ile
ENST00000373176.5:c.371C>T	ENSP00000362271.1:p.Thr124Ile
ENST00000413016.5:c.193C>T
ENST00000550143.5:c.151C>T	ENSP00000449130.1:p.Pro51Ser
ENST00000550992.1:c.*391C>T	ENSP00000448741.1:n.*391C>T
NM_000476.2:c.371C>T	NP_000467.1:p.Thr124Ile
XM_005251786.2:c.419C>T	XP_005251843.1:p.Thr140Ile
XM_011518348.1:c.371C>T	XP_011516650.1:p.Thr124Ile
XM_011518349.1:c.191C>T	XP_011516651.1:p.Thr64Ile
NM_001318121.1:c.371C>T	NP_001305050.1:p.Thr124Ile
NM_001318122.1:c.419C>T	NP_001305051.1:p.Thr140Ile
XM_017014428.1:c.371C>T	XP_016869917.1:p.Thr124Ile
XM_024447439.1:c.350C>T	XP_024303207.1:p.Thr117Ile
XM_024447440.1:c.191C>T	XP_024303208.1:p.Thr64Ile
NM_001318122.2:c.419C>T	NP_001305051.1:p.Thr140Ile
NM_000476.3:c.371C>T MANE Select	NP_000467.1:p.Thr124Ile
NR_174625.1:n.3690C>T
NR_174626.1:n.3533C>T
NR_174627.1:n.3570C>T
NR_174628.1:n.2948C>T
NR_174629.1:n.2893C>T
NR_174630.1:n.2929C>T
NR_174631.1:n.2874C>T
NR_174632.1:n.2963C>T