Canonical Allele Identifier: CA1779747378

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122423G= , CM000670.2:g.43122423G=	GRCh38
NC_000008.10:g.42977566G= , CM000670.1:g.42977566G=	GRCh37
NC_000008.9:g.43096723G=	NCBI36
NG_033235.1:g.33918G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.599G= MANE Select	ENSP00000331258.5:p.Arg200=
ENST00000614426.2:c.*395G=	ENSP00000478821.2:n.*395G=
ENST00000674646.1:c.317G=	ENSP00000501703.1:p.Arg106=
ENST00000674676.1:c.317G=	ENSP00000502544.1:p.Arg106=
ENST00000674782.1:c.*519G=	ENSP00000501683.1:n.*519G=
ENST00000674937.1:c.557G=	ENSP00000501823.1:p.Arg186=
ENST00000675322.1:c.317G=	ENSP00000502235.1:p.Arg106=
ENST00000675675.1:c.317G=	ENSP00000501793.1:p.Arg106=
ENST00000676178.1:c.*384G=	ENSP00000502007.1:n.*384G=
ENST00000676193.1:c.599G=	ENSP00000502774.1:p.Arg200=
ENST00000331373.9:c.599G=	ENSP00000331258.5:p.Arg200=
ENST00000614426.1:c.599G=	ENSP00000478821.1:p.Arg200=
NM_001277971.1:c.599G=	NP_001264900.1:p.Arg200=
NM_032237.4:c.599G=	NP_115613.1:p.Arg200=
XM_011544668.1:c.599G=	XP_011542970.1:p.Arg200=
XM_011544669.1:c.599G=	XP_011542971.1:p.Arg200=
NM_032237.5:c.599G= MANE Select	NP_115613.1:p.Arg200=
NM_001277971.2:c.599G=	NP_001264900.1:p.Arg200=