Canonical Allele Identifier: CA1779747217

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122331C= , CM000670.2:g.43122331C=	GRCh38
NC_000008.10:g.42977474C= , CM000670.1:g.42977474C=	GRCh37
NC_000008.9:g.43096631C=	NCBI36
NG_033235.1:g.33826C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.507C= MANE Select	ENSP00000331258.5:p.Tyr169=
ENST00000614426.2:c.*303C=	ENSP00000478821.2:n.*303C=
ENST00000674646.1:c.225C=	ENSP00000501703.1:p.Tyr75=
ENST00000674676.1:c.225C=	ENSP00000502544.1:p.Tyr75=
ENST00000674782.1:c.*427C=	ENSP00000501683.1:n.*427C=
ENST00000674937.1:c.465C=	ENSP00000501823.1:p.Tyr155=
ENST00000675322.1:c.225C=	ENSP00000502235.1:p.Tyr75=
ENST00000675675.1:c.225C=	ENSP00000501793.1:p.Tyr75=
ENST00000676178.1:c.*292C=	ENSP00000502007.1:n.*292C=
ENST00000676193.1:c.507C=	ENSP00000502774.1:p.Tyr169=
ENST00000331373.9:c.507C=	ENSP00000331258.5:p.Tyr169=
ENST00000614426.1:c.507C=	ENSP00000478821.1:p.Tyr169=
NM_001277971.1:c.507C=	NP_001264900.1:p.Tyr169=
NM_032237.4:c.507C=	NP_115613.1:p.Tyr169=
XM_011544668.1:c.507C=	XP_011542970.1:p.Tyr169=
XM_011544669.1:c.507C=	XP_011542971.1:p.Tyr169=
NM_032237.5:c.507C= MANE Select	NP_115613.1:p.Tyr169=
NM_001277971.2:c.507C=	NP_001264900.1:p.Tyr169=