Canonical Allele Identifier: CA1880009337

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868374T= , CM000671.2:g.127868374T=	GRCh38
NC_000009.11:g.130630653T= , CM000671.1:g.130630653T=	GRCh37
NC_000009.10:g.129670474T=	NCBI36
NG_011792.1:g.14370A=
NG_011792.2:g.14370A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.963A=
ENST00000643029.1:c.*2138A=	ENSP00000496586.1:n.*2138A=
ENST00000643338.1:c.*2027A=	ENSP00000495890.1:n.*2027A=
ENST00000644144.2:c.463A= MANE Select	ENSP00000494600.1:p.Lys155=
ENST00000645007.1:c.*2387A=	ENSP00000494773.1:n.*2387A=
ENST00000646171.1:c.*496A=	ENSP00000495484.1:n.*496A=
ENST00000223836.10:c.511A=	ENSP00000223836.10:p.Lys171=
ENST00000373156.5:c.463A=	ENSP00000362249.1:p.Lys155=
ENST00000373176.5:c.463A=	ENSP00000362271.1:p.Lys155=
ENST00000413016.5:c.285A=
ENST00000550143.5:c.243A=	ENSP00000449130.1:n.243A=
NM_000476.2:c.463A=	NP_000467.1:p.Lys155=
XM_005251786.2:c.511A=	XP_005251843.1:p.Lys171=
XM_011518348.1:c.463A=	XP_011516650.1:p.Lys155=
XM_011518349.1:c.283A=	XP_011516651.1:p.Lys95=
NM_001318121.1:c.463A=	NP_001305050.1:p.Lys155=
NM_001318122.1:c.511A=	NP_001305051.1:p.Lys171=
XM_017014428.1:c.463A=	XP_016869917.1:p.Lys155=
XM_024447439.1:c.442A=	XP_024303207.1:p.Lys148=
XM_024447440.1:c.283A=	XP_024303208.1:p.Lys95=
NM_001318122.2:c.511A=	NP_001305051.1:p.Lys171=
NM_000476.3:c.463A= MANE Select	NP_000467.1:p.Lys155=
NR_174625.1:n.3782A=
NR_174626.1:n.3625A=
NR_174627.1:n.3662A=
NR_174628.1:n.3040A=
NR_174629.1:n.2985A=
NR_174630.1:n.3021A=
NR_174631.1:n.2966A=
NR_174632.1:n.3055A=