Canonical Allele Identifier: CA371122117

Gene: POMK

Linked Data

• COSMIC: COSM3951686 ; COSM3951687
• MyVariant Identifiers: chr8:g.42977500G>T (hg19) ; chr8:g.43122357G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122357G>T , CM000670.2:g.43122357G>T	GRCh38
NC_000008.10:g.42977500G>T , CM000670.1:g.42977500G>T	GRCh37
NC_000008.9:g.43096657G>T	NCBI36
NG_033235.1:g.33852G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.533G>T MANE Select	ENSP00000331258.5:p.Arg178Met
ENST00000614426.2:c.*329G>T	ENSP00000478821.2:n.*329G>T
ENST00000674646.1:c.251G>T	ENSP00000501703.1:p.Arg84Met
ENST00000674676.1:c.251G>T	ENSP00000502544.1:p.Arg84Met
ENST00000674782.1:c.*453G>T	ENSP00000501683.1:n.*453G>T
ENST00000674937.1:c.491G>T	ENSP00000501823.1:p.Arg164Met
ENST00000675322.1:c.251G>T	ENSP00000502235.1:p.Arg84Met
ENST00000675675.1:c.251G>T	ENSP00000501793.1:p.Arg84Met
ENST00000676178.1:c.*318G>T	ENSP00000502007.1:n.*318G>T
ENST00000676193.1:c.533G>T	ENSP00000502774.1:p.Arg178Met
ENST00000331373.9:c.533G>T	ENSP00000331258.5:p.Arg178Met
ENST00000614426.1:c.533G>T	ENSP00000478821.1:p.Arg178Met
NM_001277971.1:c.533G>T	NP_001264900.1:p.Arg178Met
NM_032237.4:c.533G>T	NP_115613.1:p.Arg178Met
XM_011544668.1:c.533G>T	XP_011542970.1:p.Arg178Met
XM_011544669.1:c.533G>T	XP_011542971.1:p.Arg178Met
NM_032237.5:c.533G>T MANE Select	NP_115613.1:p.Arg178Met
NM_001277971.2:c.533G>T	NP_001264900.1:p.Arg178Met