Canonical Allele Identifier: CA1779747488

Gene: POMK

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122468A= , CM000670.2:g.43122468A=	GRCh38
NC_000008.10:g.42977611A= , CM000670.1:g.42977611A=	GRCh37
NC_000008.9:g.43096768A=	NCBI36
NG_033235.1:g.33963A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.644A= MANE Select	ENSP00000331258.5:p.Tyr215=
ENST00000614426.2:c.*440A=	ENSP00000478821.2:n.*440A=
ENST00000674646.1:c.362A=	ENSP00000501703.1:p.Tyr121=
ENST00000674676.1:c.362A=	ENSP00000502544.1:p.Tyr121=
ENST00000674782.1:c.*564A=	ENSP00000501683.1:n.*564A=
ENST00000674937.1:c.602A=	ENSP00000501823.1:p.Tyr201=
ENST00000675322.1:c.362A=	ENSP00000502235.1:p.Tyr121=
ENST00000675675.1:c.362A=	ENSP00000501793.1:p.Tyr121=
ENST00000676178.1:c.*429A=	ENSP00000502007.1:n.*429A=
ENST00000676193.1:c.644A=	ENSP00000502774.1:p.Tyr215=
ENST00000331373.9:c.644A=	ENSP00000331258.5:p.Tyr215=
ENST00000614426.1:c.644A=	ENSP00000478821.1:p.Tyr215=
NM_001277971.1:c.644A=	NP_001264900.1:p.Tyr215=
NM_032237.4:c.644A=	NP_115613.1:p.Tyr215=
XM_011544668.1:c.644A=	XP_011542970.1:p.Tyr215=
XM_011544669.1:c.644A=	XP_011542971.1:p.Tyr215=
NM_032237.5:c.644A= MANE Select	NP_115613.1:p.Tyr215=
NM_001277971.2:c.644A=	NP_001264900.1:p.Tyr215=