Canonical Allele Identifier: CA1779736230

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122903G= , CM000670.2:g.43122903G=	GRCh38
NC_000008.10:g.42978046G= , CM000670.1:g.42978046G=	GRCh37
NC_000008.9:g.43097203G=	NCBI36
NG_033235.1:g.34398G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.*26G= MANE Select	ENSP00000331258.5:n.*26G=
ENST00000614426.2:c.*875G=	ENSP00000478821.2:n.*875G=
ENST00000674646.1:c.797G=	ENSP00000501703.1:n.797G=
ENST00000674676.1:c.792+5G=	ENSP00000502544.1:n.792+5G=
ENST00000674782.1:c.*999G=	ENSP00000501683.1:n.*999G=
ENST00000674937.1:c.*26G=	ENSP00000501823.1:n.*26G=
ENST00000675322.1:c.797G=	ENSP00000502235.1:n.797G=
ENST00000675675.1:c.792+5G=	ENSP00000501793.1:n.792+5G=
ENST00000676178.1:c.*864G=	ENSP00000502007.1:n.*864G=
ENST00000676193.1:c.*26G=	ENSP00000502774.1:n.*26G=
ENST00000331373.9:c.*26G=	ENSP00000331258.5:n.*26G=
ENST00000614426.1:c.*26G=	ENSP00000478821.1:n.*26G=
NM_001277971.1:c.*26G=	NP_001264900.1:n.*26G=
NM_032237.4:c.*26G=	NP_115613.1:n.*26G=
XM_011544668.1:c.*26G=	XP_011542970.1:n.*26G=
XM_011544669.1:c.*26G=	XP_011542971.1:n.*26G=
NM_032237.5:c.*26G= MANE Select	NP_115613.1:n.*26G=
NM_001277971.2:c.*26G=	NP_001264900.1:n.*26G=