Canonical Allele Identifier: CA1880009324

Gene: AK1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868351G= , CM000671.2:g.127868351G=	GRCh38
NC_000009.11:g.130630630G= , CM000671.1:g.130630630G=	GRCh37
NC_000009.10:g.129670451G=	NCBI36
NG_011792.1:g.14393C=
NG_011792.2:g.14393C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000476274.7:n.986C=
ENST00000643029.1:c.*2161C=	ENSP00000496586.1:n.*2161C=
ENST00000643338.1:c.*2050C=	ENSP00000495890.1:n.*2050C=
ENST00000644144.2:c.486C= MANE Select	ENSP00000494600.1:p.Ala162=
ENST00000645007.1:c.*2410C=	ENSP00000494773.1:n.*2410C=
ENST00000646171.1:c.*519C=	ENSP00000495484.1:n.*519C=
ENST00000223836.10:c.534C=	ENSP00000223836.10:p.Ala178=
ENST00000373156.5:c.486C=	ENSP00000362249.1:p.Ala162=
ENST00000373176.5:c.486C=	ENSP00000362271.1:p.Ala162=
ENST00000413016.5:c.308C=
ENST00000550143.5:c.266C=	ENSP00000449130.1:n.266C=
NM_000476.2:c.486C=	NP_000467.1:p.Ala162=
XM_005251786.2:c.534C=	XP_005251843.1:p.Ala178=
XM_011518348.1:c.486C=	XP_011516650.1:p.Ala162=
XM_011518349.1:c.306C=	XP_011516651.1:p.Ala102=
NM_001318121.1:c.486C=	NP_001305050.1:p.Ala162=
NM_001318122.1:c.534C=	NP_001305051.1:p.Ala178=
XM_017014428.1:c.486C=	XP_016869917.1:p.Ala162=
XM_024447439.1:c.465C=	XP_024303207.1:p.Ala155=
XM_024447440.1:c.306C=	XP_024303208.1:p.Ala102=
NM_001318122.2:c.534C=	NP_001305051.1:p.Ala178=
NM_000476.3:c.486C= MANE Select	NP_000467.1:p.Ala162=
NR_174625.1:n.3805C=
NR_174626.1:n.3648C=
NR_174627.1:n.3685C=
NR_174628.1:n.3063C=
NR_174629.1:n.3008C=
NR_174630.1:n.3044C=
NR_174631.1:n.2989C=
NR_174632.1:n.3078C=