Canonical Allele Identifier: CA7643345

Gene: PKM

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.72208751C>T , CM000677.2:g.72208751C>T	GRCh38
NC_000015.9:g.72501092C>T , CM000677.1:g.72501092C>T	GRCh37
NC_000015.8:g.70288146C>T	NCBI36
NG_052978.1:g.27874G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698740.1:c.706G>A	ENSP00000513902.1:p.Asp236Asn
ENST00000698741.1:c.928G>A	ENSP00000513903.1:p.Asp310Asn
ENST00000335181.10:c.706G>A MANE Select	ENSP00000334983.5:p.Asp236Asn
ENST00000565154.6:c.928G>A	ENSP00000455901.2:p.Asp310Asn
ENST00000565184.6:c.811G>A	ENSP00000455736.2:p.Asp271Asn
ENST00000319622.10:c.706G>A	ENSP00000320171.6:p.Asp236Asn
ENST00000335181.9:c.706G>A	ENSP00000334983.5:p.Asp236Asn
ENST00000389093.7:c.484G>A	ENSP00000373745.4:p.Asp162Asn
ENST00000449901.6:c.661G>A	ENSP00000403365.2:p.Asp221Asn
ENST00000561609.5:c.706G>A	ENSP00000457253.1:p.Asp236Asn
ENST00000563275.1:n.212G>A
ENST00000565154.5:c.706G>A	ENSP00000455901.1:p.Asp236Asn
ENST00000565184.5:c.706G>A	ENSP00000455736.1:p.Asp236Asn
ENST00000567118.5:c.*404G>A	ENSP00000456004.1:n.*404G>A
ENST00000568459.5:c.706G>A	ENSP00000456970.1:p.Asp236Asn
ENST00000568743.1:n.495G>A
ENST00000568883.5:c.211G>A	ENSP00000456100.2:p.Asp71Asn
ENST00000569857.5:c.706G>A	ENSP00000455584.1:p.Asp236Asn
NM_001206796.1:c.928G>A	NP_001193725.1:p.Asp310Asn
NM_001206796.2:c.928G>A	NP_001193725.1:p.Asp310Asn
NM_001206797.1:c.484G>A	NP_001193726.1:p.Asp162Asn
NM_001206797.2:c.484G>A	NP_001193726.1:p.Asp162Asn
NM_001206798.1:c.661G>A	NP_001193727.1:p.Asp221Asn
NM_001206798.2:c.661G>A	NP_001193727.1:p.Asp221Asn
NM_001206799.1:c.721G>A	NP_001193728.1:p.Asp241Asn
NM_001316318.1:c.811G>A	NP_001303247.1:p.Asp271Asn
NM_002654.4:c.706G>A	NP_002645.3:p.Asp236Asn
NM_002654.5:c.706G>A	NP_002645.3:p.Asp236Asn
NM_182470.2:c.706G>A	NP_872270.1:p.Asp236Asn
NM_182470.3:c.706G>A	NP_872270.1:p.Asp236Asn
NM_182471.2:c.706G>A	NP_872271.1:p.Asp236Asn
NM_182471.3:c.706G>A	NP_872271.1:p.Asp236Asn
XM_005254443.1:c.886G>A	XP_005254500.1:p.Asp296Asn
XM_005254445.3:c.706G>A	XP_005254502.1:p.Asp236Asn
XM_006720570.1:c.928G>A	XP_006720633.1:p.Asp310Asn
XM_011521670.1:c.811G>A	XP_011519972.1:p.Asp271Asn
XM_011521672.1:c.769G>A	XP_011519974.1:p.Asp257Asn
XM_011521673.1:c.769G>A	XP_011519975.1:p.Asp257Asn
XM_005254445.5:c.706G>A	XP_005254502.1:p.Asp236Asn
XM_011521670.2:c.811G>A	XP_011519972.1:p.Asp271Asn
XM_017022313.2:c.706G>A	XP_016877802.1:p.Asp236Asn
XR_001751314.2:n.845G>A
NM_002654.6:c.706G>A MANE Select	NP_002645.3:p.Asp236Asn
NM_001206796.3:c.928G>A	NP_001193725.1:p.Asp310Asn
NM_001206799.2:c.721G>A	NP_001193728.1:p.Asp241Asn
NM_001316318.2:c.811G>A	NP_001303247.1:p.Asp271Asn
NM_182471.4:c.706G>A	NP_872271.1:p.Asp236Asn
NM_001206797.3:c.484G>A	NP_001193726.1:p.Asp162Asn
NM_001206798.3:c.661G>A	NP_001193727.1:p.Asp221Asn
NM_182470.4:c.706G>A	NP_872270.1:p.Asp236Asn