Canonical Allele Identifier: CA1779747313

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122393A= , CM000670.2:g.43122393A=	GRCh38
NC_000008.10:g.42977536A= , CM000670.1:g.42977536A=	GRCh37
NC_000008.9:g.43096693A=	NCBI36
NG_033235.1:g.33888A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.569A= MANE Select	ENSP00000331258.5:p.Asn190=
ENST00000614426.2:c.*365A=	ENSP00000478821.2:n.*365A=
ENST00000674646.1:c.287A=	ENSP00000501703.1:p.Asn96=
ENST00000674676.1:c.287A=	ENSP00000502544.1:p.Asn96=
ENST00000674782.1:c.*489A=	ENSP00000501683.1:n.*489A=
ENST00000674937.1:c.527A=	ENSP00000501823.1:p.Asn176=
ENST00000675322.1:c.287A=	ENSP00000502235.1:p.Asn96=
ENST00000675675.1:c.287A=	ENSP00000501793.1:p.Asn96=
ENST00000676178.1:c.*354A=	ENSP00000502007.1:n.*354A=
ENST00000676193.1:c.569A=	ENSP00000502774.1:p.Asn190=
ENST00000331373.9:c.569A=	ENSP00000331258.5:p.Asn190=
ENST00000614426.1:c.569A=	ENSP00000478821.1:p.Asn190=
NM_001277971.1:c.569A=	NP_001264900.1:p.Asn190=
NM_032237.4:c.569A=	NP_115613.1:p.Asn190=
XM_011544668.1:c.569A=	XP_011542970.1:p.Asn190=
XM_011544669.1:c.569A=	XP_011542971.1:p.Asn190=
NM_032237.5:c.569A= MANE Select	NP_115613.1:p.Asn190=
NM_001277971.2:c.569A=	NP_001264900.1:p.Asn190=