Canonical Allele Identifier: CA444695614

Gene: POLK

Linked Data

• MyVariant Identifiers: chr5:g.74893842A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75598017A>G , CM000667.2:g.75598017A>G	GRCh38
NC_000005.9:g.74893842A>G , CM000667.1:g.74893842A>G	GRCh37
NC_000005.8:g.74929598A>G	NCBI36
NG_051590.1:g.91268A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2612A>G MANE Select	ENSP00000241436.4:p.Ter871=
ENST00000241436.8:c.2612A>G	ENSP00000241436.4:p.Ter871=
ENST00000503479.6:c.*1135A>G	ENSP00000421997.2:n.*1135A>G
ENST00000504026.5:c.1483A>G	ENSP00000425075.1:n.1483A>G
ENST00000505069.1:n.336A>G
ENST00000505975.5:c.2726A>G	ENSP00000424859.1:n.2726A>G
ENST00000506928.5:n.2735A>G
ENST00000508526.5:c.2018A>G	ENSP00000426853.1:p.Ter673=
ENST00000509126.2:c.2440A>G	ENSP00000423532.1:n.2440A>G
ENST00000510815.6:c.*1135A>G	ENSP00000422094.2:n.*1135A>G
ENST00000514141.5:c.*1231A>G	ENSP00000423526.1:n.*1231A>G
NM_016218.2:c.2612A>G	NP_057302.1:p.Ter871=
XM_005248534.3:c.2654A>G	XP_005248591.1:p.Ter885=
XM_006714652.2:c.1367A>G	XP_006714715.1:p.Ter456=
XM_011543463.1:c.2654A>G	XP_011541765.1:p.Ter885=
XM_011543464.1:c.2654A>G	XP_011541766.1:p.Ter885=
XM_011543465.1:c.2654A>G	XP_011541767.1:p.Ter885=
XM_011543466.1:c.2654A>G	XP_011541768.1:p.Ter885=
XM_011543467.1:c.2384A>G	XP_011541769.1:p.Ter795=
XR_241784.1:n.2620A>G
XR_948273.1:n.2804A>G
NM_001345921.1:c.2414A>G	NP_001332850.1:p.Ter805=
NM_001345922.1:c.2342A>G	NP_001332851.1:p.Ter781=
NM_016218.3:c.2612A>G	NP_057302.1:p.Ter871=
NR_144315.1:n.2618A>G
XM_005248534.5:c.2654A>G	XP_005248591.1:p.Ter885=
XM_006714652.4:c.1367A>G	XP_006714715.1:p.Ter456=
XM_011543463.3:c.2654A>G	XP_011541765.1:p.Ter885=
XM_011543464.3:c.2654A>G	XP_011541766.1:p.Ter885=
XM_011543467.3:c.2384A>G	XP_011541769.1:p.Ter795=
XM_017009559.2:c.2612A>G	XP_016865048.1:p.Ter871=
XM_017009560.2:c.2612A>G	XP_016865049.1:p.Ter871=
XM_017009561.2:c.2456A>G	XP_016865050.1:p.Ter819=
XM_017009563.2:c.2342A>G	XP_016865052.1:p.Ter781=
XR_001742105.2:n.3102A>G
XR_001742107.2:n.3186A>G
XR_001742108.2:n.2720A>G
XR_241784.3:n.3144A>G
XR_948273.3:n.2804A>G
NM_001345921.2:c.2414A>G	NP_001332850.1:p.Ter805=
NM_001345922.2:c.2342A>G	NP_001332851.1:p.Ter781=
NM_001387110.2:c.2603A>G	NP_001374039.1:p.Ter868=
NM_001387111.2:c.2654A>G	NP_001374040.1:p.Ter885=
NM_001387113.2:c.2612A>G	NP_001374042.1:p.Ter871=
NM_016218.5:c.2612A>G	NP_057302.1:p.Ter871=
NR_144315.2:n.2477A>G
NR_170559.2:n.2466A>G
NR_170560.2:n.2698A>G
NM_001345921.3:c.2414A>G	NP_001332850.1:p.Ter805=
NM_001345922.3:c.2342A>G	NP_001332851.1:p.Ter781=
NM_001387110.3:c.2603A>G	NP_001374039.1:p.Ter868=
NM_001387111.3:c.2654A>G	NP_001374040.1:p.Ter885=
NM_001387113.3:c.2612A>G	NP_001374042.1:p.Ter871=
NM_001395893.1:c.2342A>G	NP_001382822.1:p.Ter781=
NM_001395894.1:c.2654A>G	NP_001382823.1:p.Ter885=
NM_001395897.1:c.2651A>G	NP_001382826.1:p.Ter884=
NM_001395899.1:c.2459A>G	NP_001382828.1:p.Ter820=
NM_001395900.1:c.2414A>G	NP_001382829.1:p.Ter805=
NM_001395901.1:c.2372A>G	NP_001382830.1:p.Ter791=
NM_001395902.1:c.2342A>G	NP_001382831.1:p.Ter781=
NM_016218.6:c.2612A>G MANE Select	NP_057302.1:p.Ter871=
NR_144315.3:n.2477A>G
NR_170559.3:n.2466A>G
NR_170560.3:n.2698A>G