Canonical Allele Identifier: CA374947452

Gene: AK1

Linked Data

• gnomAD v4: 9-127868435-C-G
• MyVariant Identifiers: chr9:g.130630714C>G (hg19) ; chr9:g.127868435C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868435C>G , CM000671.2:g.127868435C>G	GRCh38
NC_000009.11:g.130630714C>G , CM000671.1:g.130630714C>G	GRCh37
NC_000009.10:g.129670535C>G	NCBI36
NG_011792.1:g.14309G>C
NG_011792.2:g.14309G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.902G>C
ENST00000643029.1:c.*2077G>C	ENSP00000496586.1:n.*2077G>C
ENST00000643338.1:c.*1966G>C	ENSP00000495890.1:n.*1966G>C
ENST00000644144.2:c.402G>C MANE Select	ENSP00000494600.1:p.Glu134Asp
ENST00000645007.1:c.*2326G>C	ENSP00000494773.1:n.*2326G>C
ENST00000646171.1:c.*435G>C	ENSP00000495484.1:n.*435G>C
ENST00000223836.10:c.450G>C	ENSP00000223836.10:p.Glu150Asp
ENST00000373156.5:c.402G>C	ENSP00000362249.1:p.Glu134Asp
ENST00000373176.5:c.402G>C	ENSP00000362271.1:p.Glu134Asp
ENST00000413016.5:c.224G>C
ENST00000550143.5:c.182G>C	ENSP00000449130.1:n.182G>C
NM_000476.2:c.402G>C	NP_000467.1:p.Glu134Asp
XM_005251786.2:c.450G>C	XP_005251843.1:p.Glu150Asp
XM_011518348.1:c.402G>C	XP_011516650.1:p.Glu134Asp
XM_011518349.1:c.222G>C	XP_011516651.1:p.Glu74Asp
NM_001318121.1:c.402G>C	NP_001305050.1:p.Glu134Asp
NM_001318122.1:c.450G>C	NP_001305051.1:p.Glu150Asp
XM_017014428.1:c.402G>C	XP_016869917.1:p.Glu134Asp
XM_024447439.1:c.381G>C	XP_024303207.1:p.Glu127Asp
XM_024447440.1:c.222G>C	XP_024303208.1:p.Glu74Asp
NM_001318122.2:c.450G>C	NP_001305051.1:p.Glu150Asp
NM_000476.3:c.402G>C MANE Select	NP_000467.1:p.Glu134Asp
NR_174625.1:n.3721G>C
NR_174626.1:n.3564G>C
NR_174627.1:n.3601G>C
NR_174628.1:n.2979G>C
NR_174629.1:n.2924G>C
NR_174630.1:n.2960G>C
NR_174631.1:n.2905G>C
NR_174632.1:n.2994G>C