Canonical Allele Identifier: CA1779747260

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122371A= , CM000670.2:g.43122371A=	GRCh38
NC_000008.10:g.42977514A= , CM000670.1:g.42977514A=	GRCh37
NC_000008.9:g.43096671A=	NCBI36
NG_033235.1:g.33866A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.547A= MANE Select	ENSP00000331258.5:p.Met183=
ENST00000614426.2:c.*343A=	ENSP00000478821.2:n.*343A=
ENST00000674646.1:c.265A=	ENSP00000501703.1:p.Met89=
ENST00000674676.1:c.265A=	ENSP00000502544.1:p.Met89=
ENST00000674782.1:c.*467A=	ENSP00000501683.1:n.*467A=
ENST00000674937.1:c.505A=	ENSP00000501823.1:p.Met169=
ENST00000675322.1:c.265A=	ENSP00000502235.1:p.Met89=
ENST00000675675.1:c.265A=	ENSP00000501793.1:p.Met89=
ENST00000676178.1:c.*332A=	ENSP00000502007.1:n.*332A=
ENST00000676193.1:c.547A=	ENSP00000502774.1:p.Met183=
ENST00000331373.9:c.547A=	ENSP00000331258.5:p.Met183=
ENST00000614426.1:c.547A=	ENSP00000478821.1:p.Met183=
NM_001277971.1:c.547A=	NP_001264900.1:p.Met183=
NM_032237.4:c.547A=	NP_115613.1:p.Met183=
XM_011544668.1:c.547A=	XP_011542970.1:p.Met183=
XM_011544669.1:c.547A=	XP_011542971.1:p.Met183=
NM_032237.5:c.547A= MANE Select	NP_115613.1:p.Met183=
NM_001277971.2:c.547A=	NP_001264900.1:p.Met183=