Canonical Allele Identifier: CA1779747255

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122368G= , CM000670.2:g.43122368G=	GRCh38
NC_000008.10:g.42977511G= , CM000670.1:g.42977511G=	GRCh37
NC_000008.9:g.43096668G=	NCBI36
NG_033235.1:g.33863G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.544G= MANE Select	ENSP00000331258.5:p.Ala182=
ENST00000614426.2:c.*340G=	ENSP00000478821.2:n.*340G=
ENST00000674646.1:c.262G=	ENSP00000501703.1:p.Ala88=
ENST00000674676.1:c.262G=	ENSP00000502544.1:p.Ala88=
ENST00000674782.1:c.*464G=	ENSP00000501683.1:n.*464G=
ENST00000674937.1:c.502G=	ENSP00000501823.1:p.Ala168=
ENST00000675322.1:c.262G=	ENSP00000502235.1:p.Ala88=
ENST00000675675.1:c.262G=	ENSP00000501793.1:p.Ala88=
ENST00000676178.1:c.*329G=	ENSP00000502007.1:n.*329G=
ENST00000676193.1:c.544G=	ENSP00000502774.1:p.Ala182=
ENST00000331373.9:c.544G=	ENSP00000331258.5:p.Ala182=
ENST00000614426.1:c.544G=	ENSP00000478821.1:p.Ala182=
NM_001277971.1:c.544G=	NP_001264900.1:p.Ala182=
NM_032237.4:c.544G=	NP_115613.1:p.Ala182=
XM_011544668.1:c.544G=	XP_011542970.1:p.Ala182=
XM_011544669.1:c.544G=	XP_011542971.1:p.Ala182=
NM_032237.5:c.544G= MANE Select	NP_115613.1:p.Ala182=
NM_001277971.2:c.544G=	NP_001264900.1:p.Ala182=