Canonical Allele Identifier: CA860199997

Gene: AK1

Linked Data

• dbSNP Id: rs1404191771
• gnomAD v3: 9-127868200-G-C
• gnomAD v4: 9-127868200-G-C
• MyVariant Identifiers: chr9:g.130630479G>C (hg19) ; chr9:g.127868200G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868200G>C , CM000671.2:g.127868200G>C	GRCh38
NC_000009.11:g.130630479G>C , CM000671.1:g.130630479G>C	GRCh37
NC_000009.10:g.129670300G>C	NCBI36
NG_011792.1:g.14544C>G
NG_011792.2:g.14544C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.1016+121C>G
ENST00000643029.1:c.*2191+121C>G	ENSP00000496586.1:n.*2191+121C>G
ENST00000643338.1:c.*2080+121C>G	ENSP00000495890.1:n.*2080+121C>G
ENST00000644144.2:c.516+121C>G MANE Select	ENSP00000494600.1:n.516+121C>G
ENST00000645007.1:c.*2440+121C>G	ENSP00000494773.1:n.*2440+121C>G
ENST00000646171.1:c.*549+121C>G	ENSP00000495484.1:n.*549+121C>G
ENST00000223836.10:c.564+121C>G	ENSP00000223836.10:n.564+121C>G
ENST00000373156.5:c.516+121C>G	ENSP00000362249.1:n.516+121C>G
ENST00000373176.5:c.516+121C>G	ENSP00000362271.1:n.516+121C>G
ENST00000413016.5:c.338+121C>G
ENST00000550143.5:c.296+121C>G	ENSP00000449130.1:n.296+121C>G
NM_000476.2:c.516+121C>G	NP_000467.1:n.516+121C>G
XM_005251786.2:c.564+121C>G	XP_005251843.1:n.564+121C>G
XM_011518348.1:c.516+121C>G	XP_011516650.1:n.516+121C>G
XM_011518349.1:c.336+121C>G	XP_011516651.1:n.336+121C>G
NM_001318121.1:c.516+121C>G	NP_001305050.1:n.516+121C>G
NM_001318122.1:c.564+121C>G	NP_001305051.1:n.564+121C>G
XM_017014428.1:c.516+121C>G	XP_016869917.1:n.516+121C>G
XM_024447439.1:c.495+121C>G	XP_024303207.1:n.495+121C>G
XM_024447440.1:c.336+121C>G	XP_024303208.1:n.336+121C>G
NM_001318122.2:c.564+121C>G	NP_001305051.1:n.564+121C>G
NM_000476.3:c.516+121C>G MANE Select	NP_000467.1:n.516+121C>G
NR_174625.1:n.3835+121C>G
NR_174626.1:n.3678+121C>G
NR_174627.1:n.3715+121C>G
NR_174628.1:n.3093+121C>G
NR_174629.1:n.3038+121C>G
NR_174630.1:n.3074+121C>G
NR_174631.1:n.3019+121C>G
NR_174632.1:n.3108+121C>G