Canonical Allele Identifier: CA1779747503

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122481C= , CM000670.2:g.43122481C=	GRCh38
NC_000008.10:g.42977624C= , CM000670.1:g.42977624C=	GRCh37
NC_000008.9:g.43096781C=	NCBI36
NG_033235.1:g.33976C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.657C= MANE Select	ENSP00000331258.5:p.Ser219=
ENST00000614426.2:c.*453C=	ENSP00000478821.2:n.*453C=
ENST00000674646.1:c.375C=	ENSP00000501703.1:p.Ser125=
ENST00000674676.1:c.375C=	ENSP00000502544.1:p.Ser125=
ENST00000674782.1:c.*577C=	ENSP00000501683.1:n.*577C=
ENST00000674937.1:c.615C=	ENSP00000501823.1:p.Ser205=
ENST00000675322.1:c.375C=	ENSP00000502235.1:p.Ser125=
ENST00000675675.1:c.375C=	ENSP00000501793.1:p.Ser125=
ENST00000676178.1:c.*442C=	ENSP00000502007.1:n.*442C=
ENST00000676193.1:c.657C=	ENSP00000502774.1:p.Ser219=
ENST00000331373.9:c.657C=	ENSP00000331258.5:p.Ser219=
ENST00000614426.1:c.657C=	ENSP00000478821.1:p.Ser219=
NM_001277971.1:c.657C=	NP_001264900.1:p.Ser219=
NM_032237.4:c.657C=	NP_115613.1:p.Ser219=
XM_011544668.1:c.657C=	XP_011542970.1:p.Ser219=
XM_011544669.1:c.657C=	XP_011542971.1:p.Ser219=
NM_032237.5:c.657C= MANE Select	NP_115613.1:p.Ser219=
NM_001277971.2:c.657C=	NP_001264900.1:p.Ser219=