Canonical Allele Identifier: CA2691812689
Gene: AK1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.127868524C>T , CM000671.2:g.127868524C>T GRCh38
NC_000009.11:g.130630803C>T , CM000671.1:g.130630803C>T GRCh37
NC_000009.10:g.129670624C>T NCBI36
NG_011792.1:g.14220G>A
NG_011792.2:g.14220G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000476274.7:n.825-12G>A
ENST00000643029.1:c.*2000-12G>A ENSP00000496586.1:n.*2000-12G>A
ENST00000643338.1:c.*1889-12G>A ENSP00000495890.1:n.*1889-12G>A
ENST00000644144.2:c.325-12G>A MANE Select ENSP00000494600.1:n.325-12G>A
ENST00000645007.1:c.*2249-12G>A ENSP00000494773.1:n.*2249-12G>A
ENST00000646171.1:c.*358-12G>A ENSP00000495484.1:n.*358-12G>A
ENST00000223836.10:c.373-12G>A ENSP00000223836.10:n.373-12G>A
ENST00000373156.5:c.325-12G>A ENSP00000362249.1:n.325-12G>A
ENST00000373176.5:c.325-12G>A ENSP00000362271.1:n.325-12G>A
ENST00000413016.5:c.147-12G>A
ENST00000550143.5:c.142-49G>A ENSP00000449130.1:n.142-49G>A
ENST00000550992.1:c.*345-12G>A ENSP00000448741.1:n.*345-12G>A
NM_000476.2:c.325-12G>A NP_000467.1:n.325-12G>A
XM_005251786.2:c.373-12G>A XP_005251843.1:n.373-12G>A
XM_011518348.1:c.325-12G>A XP_011516650.1:n.325-12G>A
XM_011518349.1:c.145-12G>A XP_011516651.1:n.145-12G>A
NM_001318121.1:c.325-12G>A NP_001305050.1:n.325-12G>A
NM_001318122.1:c.373-12G>A NP_001305051.1:n.373-12G>A
XM_017014428.1:c.325-12G>A XP_016869917.1:n.325-12G>A
XM_024447439.1:c.304-12G>A XP_024303207.1:n.304-12G>A
XM_024447440.1:c.145-12G>A XP_024303208.1:n.145-12G>A
NM_001318122.2:c.373-12G>A NP_001305051.1:n.373-12G>A
NM_000476.3:c.325-12G>A MANE Select NP_000467.1:n.325-12G>A
NR_174625.1:n.3644-12G>A
NR_174626.1:n.3524-49G>A
NR_174627.1:n.3524-12G>A
NR_174628.1:n.2902-12G>A
NR_174629.1:n.2847-12G>A
NR_174630.1:n.2883-12G>A
NR_174631.1:n.2828-12G>A
NR_174632.1:n.2917-12G>A