Canonical Allele Identifier: CA7643457

Gene: PKM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72210408C>T , CM000677.2:g.72210408C>T	GRCh38
NC_000015.9:g.72502749C>T , CM000677.1:g.72502749C>T	GRCh37
NC_000015.8:g.70289803C>T	NCBI36
NG_052978.1:g.26217G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698740.1:c.317G>A	ENSP00000513902.1:p.Arg106Gln
ENST00000698741.1:c.539G>A	ENSP00000513903.1:p.Arg180Gln
ENST00000335181.10:c.317G>A MANE Select	ENSP00000334983.5:p.Arg106Gln
ENST00000565154.6:c.539G>A	ENSP00000455901.2:p.Arg180Gln
ENST00000565184.6:c.422G>A	ENSP00000455736.2:p.Arg141Gln
ENST00000319622.10:c.317G>A	ENSP00000320171.6:p.Arg106Gln
ENST00000335181.9:c.317G>A	ENSP00000334983.5:p.Arg106Gln
ENST00000389093.7:c.172-564G>A	ENSP00000373745.4:n.172-564G>A
ENST00000449901.6:c.272G>A	ENSP00000403365.2:p.Arg91Gln
ENST00000561609.5:c.317G>A	ENSP00000457253.1:p.Arg106Gln
ENST00000562784.1:n.114G>A
ENST00000562997.5:c.317G>A	ENSP00000457830.1:p.Arg106Gln
ENST00000564178.5:c.317G>A	ENSP00000457198.1:p.Arg106Gln
ENST00000564276.1:n.405G>A
ENST00000565154.5:c.317G>A	ENSP00000455901.1:p.Arg106Gln
ENST00000565184.5:c.317G>A	ENSP00000455736.1:p.Arg106Gln
ENST00000567087.5:c.317G>A	ENSP00000456984.1:p.Arg106Gln
ENST00000567118.5:c.*15G>A	ENSP00000456004.1:n.*15G>A
ENST00000568459.5:c.317G>A	ENSP00000456970.1:p.Arg106Gln
ENST00000568883.5:c.120-1566G>A	ENSP00000456100.2:n.120-1566G>A
ENST00000569857.5:c.317G>A	ENSP00000455584.1:p.Arg106Gln
NM_001206796.1:c.539G>A	NP_001193725.1:p.Arg180Gln
NM_001206796.2:c.539G>A	NP_001193725.1:p.Arg180Gln
NM_001206797.1:c.172-564G>A	NP_001193726.1:n.172-564G>A
NM_001206797.2:c.172-564G>A	NP_001193726.1:n.172-564G>A
NM_001206798.1:c.272G>A	NP_001193727.1:p.Arg91Gln
NM_001206798.2:c.272G>A	NP_001193727.1:p.Arg91Gln
NM_001206799.1:c.332G>A	NP_001193728.1:p.Arg111Gln
NM_001316318.1:c.422G>A	NP_001303247.1:p.Arg141Gln
NM_002654.4:c.317G>A	NP_002645.3:p.Arg106Gln
NM_002654.5:c.317G>A	NP_002645.3:p.Arg106Gln
NM_182470.2:c.317G>A	NP_872270.1:p.Arg106Gln
NM_182470.3:c.317G>A	NP_872270.1:p.Arg106Gln
NM_182471.2:c.317G>A	NP_872271.1:p.Arg106Gln
NM_182471.3:c.317G>A	NP_872271.1:p.Arg106Gln
XM_005254443.1:c.497G>A	XP_005254500.1:p.Arg166Gln
XM_005254445.3:c.317G>A	XP_005254502.1:p.Arg106Gln
XM_006720570.1:c.539G>A	XP_006720633.1:p.Arg180Gln
XM_011521670.1:c.422G>A	XP_011519972.1:p.Arg141Gln
XM_011521672.1:c.380G>A	XP_011519974.1:p.Arg127Gln
XM_011521673.1:c.380G>A	XP_011519975.1:p.Arg127Gln
XM_005254445.5:c.317G>A	XP_005254502.1:p.Arg106Gln
XM_011521670.2:c.422G>A	XP_011519972.1:p.Arg141Gln
XM_017022313.2:c.317G>A	XP_016877802.1:p.Arg106Gln
XR_001751314.2:n.456G>A
NM_002654.6:c.317G>A MANE Select	NP_002645.3:p.Arg106Gln
NM_001206796.3:c.539G>A	NP_001193725.1:p.Arg180Gln
NM_001206799.2:c.332G>A	NP_001193728.1:p.Arg111Gln
NM_001316318.2:c.422G>A	NP_001303247.1:p.Arg141Gln
NM_182471.4:c.317G>A	NP_872271.1:p.Arg106Gln
NM_001206797.3:c.172-564G>A	NP_001193726.1:n.172-564G>A
NM_001206798.3:c.272G>A	NP_001193727.1:p.Arg91Gln
NM_182470.4:c.317G>A	NP_872270.1:p.Arg106Gln