Canonical Allele Identifier: CA1556178852

Gene: POLK

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597863T= , CM000667.2:g.75597863T=	GRCh38
NC_000005.9:g.74893688T= , CM000667.1:g.74893688T=	GRCh37
NC_000005.8:g.74929444T=	NCBI36
NG_051590.1:g.91114T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000241436.9:c.2529-71T= MANE Select	ENSP00000241436.4:n.2529-71T=
ENST00000241436.8:c.2529-71T=	ENSP00000241436.4:n.2529-71T=
ENST00000502567.1:n.374-71T=
ENST00000503479.6:c.*1052-71T=	ENSP00000421997.2:n.*1052-71T=
ENST00000504026.5:c.1400-71T=	ENSP00000425075.1:n.1400-71T=
ENST00000505069.1:n.182T=
ENST00000505975.5:c.2643-71T=	ENSP00000424859.1:n.2643-71T=
ENST00000506928.5:n.2652-71T=
ENST00000508526.5:c.1935-71T=	ENSP00000426853.1:n.1935-71T=
ENST00000509126.2:c.2357-71T=	ENSP00000423532.1:n.2357-71T=
ENST00000510815.6:c.*1052-71T=	ENSP00000422094.2:n.*1052-71T=
ENST00000511527.5:c.1514-71T=	ENSP00000420997.1:n.1514-71T=
ENST00000514141.5:c.*1148-71T=	ENSP00000423526.1:n.*1148-71T=
NM_016218.2:c.2529-71T=	NP_057302.1:n.2529-71T=
XM_005248534.3:c.2571-71T=	XP_005248591.1:n.2571-71T=
XM_006714652.2:c.1284-71T=	XP_006714715.1:n.1284-71T=
XM_011543463.1:c.2571-71T=	XP_011541765.1:n.2571-71T=
XM_011543464.1:c.2571-71T=	XP_011541766.1:n.2571-71T=
XM_011543465.1:c.2571-71T=	XP_011541767.1:n.2571-71T=
XM_011543466.1:c.2571-71T=	XP_011541768.1:n.2571-71T=
XM_011543467.1:c.2301-71T=	XP_011541769.1:n.2301-71T=
XR_241784.1:n.2537-71T=
XR_948273.1:n.2721-71T=
NM_001345921.1:c.2331-71T=	NP_001332850.1:n.2331-71T=
NM_001345922.1:c.2259-71T=	NP_001332851.1:n.2259-71T=
NM_016218.3:c.2529-71T=	NP_057302.1:n.2529-71T=
NR_144315.1:n.2535-71T=
XM_005248534.5:c.2571-71T=	XP_005248591.1:n.2571-71T=
XM_006714652.4:c.1284-71T=	XP_006714715.1:n.1284-71T=
XM_011543463.3:c.2571-71T=	XP_011541765.1:n.2571-71T=
XM_011543464.3:c.2571-71T=	XP_011541766.1:n.2571-71T=
XM_011543467.3:c.2301-71T=	XP_011541769.1:n.2301-71T=
XM_017009559.2:c.2529-71T=	XP_016865048.1:n.2529-71T=
XM_017009560.2:c.2529-71T=	XP_016865049.1:n.2529-71T=
XM_017009561.2:c.2373-71T=	XP_016865050.1:n.2373-71T=
XM_017009563.2:c.2259-71T=	XP_016865052.1:n.2259-71T=
XR_001742105.2:n.3019-71T=
XR_001742107.2:n.3103-71T=
XR_001742108.2:n.2637-71T=
XR_241784.3:n.3061-71T=
XR_948273.3:n.2721-71T=
NM_001345921.2:c.2331-71T=	NP_001332850.1:n.2331-71T=
NM_001345922.2:c.2259-71T=	NP_001332851.1:n.2259-71T=
NM_001387110.2:c.2520-71T=	NP_001374039.1:n.2520-71T=
NM_001387111.2:c.2571-71T=	NP_001374040.1:n.2571-71T=
NM_001387113.2:c.2529-71T=	NP_001374042.1:n.2529-71T=
NM_016218.5:c.2529-71T=	NP_057302.1:n.2529-71T=
NR_144315.2:n.2394-71T=
NR_170559.2:n.2383-71T=
NR_170560.2:n.2615-71T=
NM_001345921.3:c.2331-71T=	NP_001332850.1:n.2331-71T=
NM_001345922.3:c.2259-71T=	NP_001332851.1:n.2259-71T=
NM_001387110.3:c.2520-71T=	NP_001374039.1:n.2520-71T=
NM_001387111.3:c.2571-71T=	NP_001374040.1:n.2571-71T=
NM_001387113.3:c.2529-71T=	NP_001374042.1:n.2529-71T=
NM_001395893.1:c.2259-71T=	NP_001382822.1:n.2259-71T=
NM_001395894.1:c.2571-71T=	NP_001382823.1:n.2571-71T=
NM_001395897.1:c.2568-71T=	NP_001382826.1:n.2568-71T=
NM_001395899.1:c.2376-71T=	NP_001382828.1:n.2376-71T=
NM_001395900.1:c.2331-71T=	NP_001382829.1:n.2331-71T=
NM_001395901.1:c.2289-71T=	NP_001382830.1:n.2289-71T=
NM_001395902.1:c.2259-71T=	NP_001382831.1:n.2259-71T=
NM_016218.6:c.2529-71T= MANE Select	NP_057302.1:n.2529-71T=
NR_144315.3:n.2394-71T=
NR_170559.3:n.2383-71T=
NR_170560.3:n.2615-71T=