Canonical Allele Identifier: CA374946922

Gene: AK1

Linked Data

• MyVariant Identifiers: chr9:g.130630634A>T (hg19) ; chr9:g.127868355A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.127868355A>T , CM000671.2:g.127868355A>T	GRCh38
NC_000009.11:g.130630634A>T , CM000671.1:g.130630634A>T	GRCh37
NC_000009.10:g.129670455A>T	NCBI36
NG_011792.1:g.14389T>A
NG_011792.2:g.14389T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476274.7:n.982T>A
ENST00000643029.1:c.*2157T>A	ENSP00000496586.1:n.*2157T>A
ENST00000643338.1:c.*2046T>A	ENSP00000495890.1:n.*2046T>A
ENST00000644144.2:c.482T>A MANE Select	ENSP00000494600.1:p.Ile161Asn
ENST00000645007.1:c.*2406T>A	ENSP00000494773.1:n.*2406T>A
ENST00000646171.1:c.*515T>A	ENSP00000495484.1:n.*515T>A
ENST00000223836.10:c.530T>A	ENSP00000223836.10:p.Ile177Asn
ENST00000373156.5:c.482T>A	ENSP00000362249.1:p.Ile161Asn
ENST00000373176.5:c.482T>A	ENSP00000362271.1:p.Ile161Asn
ENST00000413016.5:c.304T>A
ENST00000550143.5:c.262T>A	ENSP00000449130.1:n.262T>A
NM_000476.2:c.482T>A	NP_000467.1:p.Ile161Asn
XM_005251786.2:c.530T>A	XP_005251843.1:p.Ile177Asn
XM_011518348.1:c.482T>A	XP_011516650.1:p.Ile161Asn
XM_011518349.1:c.302T>A	XP_011516651.1:p.Ile101Asn
NM_001318121.1:c.482T>A	NP_001305050.1:p.Ile161Asn
NM_001318122.1:c.530T>A	NP_001305051.1:p.Ile177Asn
XM_017014428.1:c.482T>A	XP_016869917.1:p.Ile161Asn
XM_024447439.1:c.461T>A	XP_024303207.1:p.Ile154Asn
XM_024447440.1:c.302T>A	XP_024303208.1:p.Ile101Asn
NM_001318122.2:c.530T>A	NP_001305051.1:p.Ile177Asn
NM_000476.3:c.482T>A MANE Select	NP_000467.1:p.Ile161Asn
NR_174625.1:n.3801T>A
NR_174626.1:n.3644T>A
NR_174627.1:n.3681T>A
NR_174628.1:n.3059T>A
NR_174629.1:n.3004T>A
NR_174630.1:n.3040T>A
NR_174631.1:n.2985T>A
NR_174632.1:n.3074T>A