Canonical Allele Identifier: CA374947692

Gene: AK1

Linked Data

• gnomAD v4: 9-127868478-G-A
• MyVariant Identifiers: chr9:g.130630757G>A (hg19) ; chr9:g.127868478G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868478G>A , CM000671.2:g.127868478G>A	GRCh38
NC_000009.11:g.130630757G>A , CM000671.1:g.130630757G>A	GRCh37
NC_000009.10:g.129670578G>A	NCBI36
NG_011792.1:g.14266C>T
NG_011792.2:g.14266C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.859C>T
ENST00000643029.1:c.*2034C>T	ENSP00000496586.1:n.*2034C>T
ENST00000643338.1:c.*1923C>T	ENSP00000495890.1:n.*1923C>T
ENST00000644144.2:c.359C>T MANE Select	ENSP00000494600.1:p.Ala120Val
ENST00000645007.1:c.*2283C>T	ENSP00000494773.1:n.*2283C>T
ENST00000646171.1:c.*392C>T	ENSP00000495484.1:n.*392C>T
ENST00000223836.10:c.407C>T	ENSP00000223836.10:p.Ala136Val
ENST00000373156.5:c.359C>T	ENSP00000362249.1:p.Ala120Val
ENST00000373176.5:c.359C>T	ENSP00000362271.1:p.Ala120Val
ENST00000413016.5:c.181C>T
ENST00000550143.5:c.142-3C>T	ENSP00000449130.1:n.142-3C>T
ENST00000550992.1:c.*379C>T	ENSP00000448741.1:n.*379C>T
NM_000476.2:c.359C>T	NP_000467.1:p.Ala120Val
XM_005251786.2:c.407C>T	XP_005251843.1:p.Ala136Val
XM_011518348.1:c.359C>T	XP_011516650.1:p.Ala120Val
XM_011518349.1:c.179C>T	XP_011516651.1:p.Ala60Val
NM_001318121.1:c.359C>T	NP_001305050.1:p.Ala120Val
NM_001318122.1:c.407C>T	NP_001305051.1:p.Ala136Val
XM_017014428.1:c.359C>T	XP_016869917.1:p.Ala120Val
XM_024447439.1:c.338C>T	XP_024303207.1:p.Ala113Val
XM_024447440.1:c.179C>T	XP_024303208.1:p.Ala60Val
NM_001318122.2:c.407C>T	NP_001305051.1:p.Ala136Val
NM_000476.3:c.359C>T MANE Select	NP_000467.1:p.Ala120Val
NR_174625.1:n.3678C>T
NR_174626.1:n.3524-3C>T
NR_174627.1:n.3558C>T
NR_174628.1:n.2936C>T
NR_174629.1:n.2881C>T
NR_174630.1:n.2917C>T
NR_174631.1:n.2862C>T
NR_174632.1:n.2951C>T