Canonical Allele Identifier: CA371122708

Gene: POMK

Linked Data

• MyVariant Identifiers: chr8:g.42977774C>A (hg19) ; chr8:g.43122631C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122631C>A , CM000670.2:g.43122631C>A	GRCh38
NC_000008.10:g.42977774C>A , CM000670.1:g.42977774C>A	GRCh37
NC_000008.9:g.43096931C>A	NCBI36
NG_033235.1:g.34126C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.807C>A MANE Select	ENSP00000331258.5:p.His269Gln
ENST00000614426.2:c.*603C>A	ENSP00000478821.2:n.*603C>A
ENST00000674646.1:c.525C>A	ENSP00000501703.1:p.His175Gln
ENST00000674676.1:c.525C>A	ENSP00000502544.1:p.His175Gln
ENST00000674782.1:c.*727C>A	ENSP00000501683.1:n.*727C>A
ENST00000674937.1:c.765C>A	ENSP00000501823.1:p.His255Gln
ENST00000675322.1:c.525C>A	ENSP00000502235.1:p.His175Gln
ENST00000675675.1:c.525C>A	ENSP00000501793.1:p.His175Gln
ENST00000676178.1:c.*592C>A	ENSP00000502007.1:n.*592C>A
ENST00000676193.1:c.807C>A	ENSP00000502774.1:p.His269Gln
ENST00000331373.9:c.807C>A	ENSP00000331258.5:p.His269Gln
ENST00000614426.1:c.807C>A	ENSP00000478821.1:p.His269Gln
NM_001277971.1:c.807C>A	NP_001264900.1:p.His269Gln
NM_032237.4:c.807C>A	NP_115613.1:p.His269Gln
XM_011544668.1:c.807C>A	XP_011542970.1:p.His269Gln
XM_011544669.1:c.807C>A	XP_011542971.1:p.His269Gln
NM_032237.5:c.807C>A MANE Select	NP_115613.1:p.His269Gln
NM_001277971.2:c.807C>A	NP_001264900.1:p.His269Gln