Canonical Allele Identifier: CA360155042

Gene: POLK

Linked Data

• gnomAD v4: 5-75597987-C-A
• MyVariant Identifiers: chr5:g.74893812C>A (hg19) ; chr5:g.75597987C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.75597987C>A , CM000667.2:g.75597987C>A	GRCh38
NC_000005.9:g.74893812C>A , CM000667.1:g.74893812C>A	GRCh37
NC_000005.8:g.74929568C>A	NCBI36
NG_051590.1:g.91238C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000241436.9:c.2582C>A MANE Select	ENSP00000241436.4:p.Pro861His
ENST00000241436.8:c.2582C>A	ENSP00000241436.4:p.Pro861His
ENST00000502567.1:n.427C>A
ENST00000503479.6:c.*1105C>A	ENSP00000421997.2:n.*1105C>A
ENST00000504026.5:c.1453C>A	ENSP00000425075.1:n.1453C>A
ENST00000505069.1:n.306C>A
ENST00000505975.5:c.2696C>A	ENSP00000424859.1:n.2696C>A
ENST00000506928.5:n.2705C>A
ENST00000508526.5:c.1988C>A	ENSP00000426853.1:p.Pro663His
ENST00000509126.2:c.2410C>A	ENSP00000423532.1:n.2410C>A
ENST00000510815.6:c.*1105C>A	ENSP00000422094.2:n.*1105C>A
ENST00000511527.5:c.1567C>A	ENSP00000420997.1:n.1567C>A
ENST00000514141.5:c.*1201C>A	ENSP00000423526.1:n.*1201C>A
NM_016218.2:c.2582C>A	NP_057302.1:p.Pro861His
XM_005248534.3:c.2624C>A	XP_005248591.1:p.Pro875His
XM_006714652.2:c.1337C>A	XP_006714715.1:p.Pro446His
XM_011543463.1:c.2624C>A	XP_011541765.1:p.Pro875His
XM_011543464.1:c.2624C>A	XP_011541766.1:p.Pro875His
XM_011543465.1:c.2624C>A	XP_011541767.1:p.Pro875His
XM_011543466.1:c.2624C>A	XP_011541768.1:p.Pro875His
XM_011543467.1:c.2354C>A	XP_011541769.1:p.Pro785His
XR_241784.1:n.2590C>A
XR_948273.1:n.2774C>A
NM_001345921.1:c.2384C>A	NP_001332850.1:p.Pro795His
NM_001345922.1:c.2312C>A	NP_001332851.1:p.Pro771His
NM_016218.3:c.2582C>A	NP_057302.1:p.Pro861His
NR_144315.1:n.2588C>A
XM_005248534.5:c.2624C>A	XP_005248591.1:p.Pro875His
XM_006714652.4:c.1337C>A	XP_006714715.1:p.Pro446His
XM_011543463.3:c.2624C>A	XP_011541765.1:p.Pro875His
XM_011543464.3:c.2624C>A	XP_011541766.1:p.Pro875His
XM_011543467.3:c.2354C>A	XP_011541769.1:p.Pro785His
XM_017009559.2:c.2582C>A	XP_016865048.1:p.Pro861His
XM_017009560.2:c.2582C>A	XP_016865049.1:p.Pro861His
XM_017009561.2:c.2426C>A	XP_016865050.1:p.Pro809His
XM_017009563.2:c.2312C>A	XP_016865052.1:p.Pro771His
XR_001742105.2:n.3072C>A
XR_001742107.2:n.3156C>A
XR_001742108.2:n.2690C>A
XR_241784.3:n.3114C>A
XR_948273.3:n.2774C>A
NM_001345921.2:c.2384C>A	NP_001332850.1:p.Pro795His
NM_001345922.2:c.2312C>A	NP_001332851.1:p.Pro771His
NM_001387110.2:c.2573C>A	NP_001374039.1:p.Pro858His
NM_001387111.2:c.2624C>A	NP_001374040.1:p.Pro875His
NM_001387113.2:c.2582C>A	NP_001374042.1:p.Pro861His
NM_016218.5:c.2582C>A	NP_057302.1:p.Pro861His
NR_144315.2:n.2447C>A
NR_170559.2:n.2436C>A
NR_170560.2:n.2668C>A
NM_001345921.3:c.2384C>A	NP_001332850.1:p.Pro795His
NM_001345922.3:c.2312C>A	NP_001332851.1:p.Pro771His
NM_001387110.3:c.2573C>A	NP_001374039.1:p.Pro858His
NM_001387111.3:c.2624C>A	NP_001374040.1:p.Pro875His
NM_001387113.3:c.2582C>A	NP_001374042.1:p.Pro861His
NM_001395893.1:c.2312C>A	NP_001382822.1:p.Pro771His
NM_001395894.1:c.2624C>A	NP_001382823.1:p.Pro875His
NM_001395897.1:c.2621C>A	NP_001382826.1:p.Pro874His
NM_001395899.1:c.2429C>A	NP_001382828.1:p.Pro810His
NM_001395900.1:c.2384C>A	NP_001382829.1:p.Pro795His
NM_001395901.1:c.2342C>A	NP_001382830.1:p.Pro781His
NM_001395902.1:c.2312C>A	NP_001382831.1:p.Pro771His
NM_016218.6:c.2582C>A MANE Select	NP_057302.1:p.Pro861His
NR_144315.3:n.2447C>A
NR_170559.3:n.2436C>A
NR_170560.3:n.2668C>A