Canonical Allele Identifier: CA374947187

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630672C>G (hg19) ; chr9:g.127868393C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868393C>G , CM000671.2:g.127868393C>G	GRCh38
NC_000009.11:g.130630672C>G , CM000671.1:g.130630672C>G	GRCh37
NC_000009.10:g.129670493C>G	NCBI36
NG_011792.1:g.14351G>C
NG_011792.2:g.14351G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.944G>C
ENST00000643029.1:c.*2119G>C	ENSP00000496586.1:n.*2119G>C
ENST00000643338.1:c.*2008G>C	ENSP00000495890.1:n.*2008G>C
ENST00000644144.2:c.444G>C MANE Select	ENSP00000494600.1:p.Lys148Asn
ENST00000645007.1:c.*2368G>C	ENSP00000494773.1:n.*2368G>C
ENST00000646171.1:c.*477G>C	ENSP00000495484.1:n.*477G>C
ENST00000223836.10:c.492G>C	ENSP00000223836.10:p.Lys164Asn
ENST00000373156.5:c.444G>C	ENSP00000362249.1:p.Lys148Asn
ENST00000373176.5:c.444G>C	ENSP00000362271.1:p.Lys148Asn
ENST00000413016.5:c.266G>C
ENST00000550143.5:c.224G>C	ENSP00000449130.1:n.224G>C
NM_000476.2:c.444G>C	NP_000467.1:p.Lys148Asn
XM_005251786.2:c.492G>C	XP_005251843.1:p.Lys164Asn
XM_011518348.1:c.444G>C	XP_011516650.1:p.Lys148Asn
XM_011518349.1:c.264G>C	XP_011516651.1:p.Lys88Asn
NM_001318121.1:c.444G>C	NP_001305050.1:p.Lys148Asn
NM_001318122.1:c.492G>C	NP_001305051.1:p.Lys164Asn
XM_017014428.1:c.444G>C	XP_016869917.1:p.Lys148Asn
XM_024447439.1:c.423G>C	XP_024303207.1:p.Lys141Asn
XM_024447440.1:c.264G>C	XP_024303208.1:p.Lys88Asn
NM_001318122.2:c.492G>C	NP_001305051.1:p.Lys164Asn
NM_000476.3:c.444G>C MANE Select	NP_000467.1:p.Lys148Asn
NR_174625.1:n.3763G>C
NR_174626.1:n.3606G>C
NR_174627.1:n.3643G>C
NR_174628.1:n.3021G>C
NR_174629.1:n.2966G>C
NR_174630.1:n.3002G>C
NR_174631.1:n.2947G>C
NR_174632.1:n.3036G>C