Canonical Allele Identifier: CA460787432

Gene: POMK

Linked Data

• MyVariant Identifiers: chr8:g.42977876A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122733A>C , CM000670.2:g.43122733A>C	GRCh38
NC_000008.10:g.42977876A>C , CM000670.1:g.42977876A>C	GRCh37
NC_000008.9:g.43097033A>C	NCBI36
NG_033235.1:g.34228A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000331373.10:c.909A>C MANE Select	ENSP00000331258.5:p.Arg303=
ENST00000614426.2:c.*705A>C	ENSP00000478821.2:n.*705A>C
ENST00000674646.1:c.627A>C	ENSP00000501703.1:p.Arg209=
ENST00000674676.1:c.627A>C	ENSP00000502544.1:p.Arg209=
ENST00000674782.1:c.*829A>C	ENSP00000501683.1:n.*829A>C
ENST00000674937.1:c.867A>C	ENSP00000501823.1:p.Arg289=
ENST00000675322.1:c.627A>C	ENSP00000502235.1:p.Arg209=
ENST00000675675.1:c.627A>C	ENSP00000501793.1:p.Arg209=
ENST00000676178.1:c.*694A>C	ENSP00000502007.1:n.*694A>C
ENST00000676193.1:c.909A>C	ENSP00000502774.1:p.Arg303=
ENST00000331373.9:c.909A>C	ENSP00000331258.5:p.Arg303=
ENST00000614426.1:c.909A>C	ENSP00000478821.1:p.Arg303=
NM_001277971.1:c.909A>C	NP_001264900.1:p.Arg303=
NM_032237.4:c.909A>C	NP_115613.1:p.Arg303=
XM_011544668.1:c.909A>C	XP_011542970.1:p.Arg303=
XM_011544669.1:c.909A>C	XP_011542971.1:p.Arg303=
NM_032237.5:c.909A>C MANE Select	NP_115613.1:p.Arg303=
NM_001277971.2:c.909A>C	NP_001264900.1:p.Arg303=