Canonical Allele Identifier: CA371122695

Gene: POMK

Linked Data

• MyVariant Identifiers: chr8:g.42977769T>C (hg19) ; chr8:g.43122626T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122626T>C , CM000670.2:g.43122626T>C	GRCh38
NC_000008.10:g.42977769T>C , CM000670.1:g.42977769T>C	GRCh37
NC_000008.9:g.43096926T>C	NCBI36
NG_033235.1:g.34121T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.802T>C MANE Select	ENSP00000331258.5:p.Phe268Leu
ENST00000614426.2:c.*598T>C	ENSP00000478821.2:n.*598T>C
ENST00000674646.1:c.520T>C	ENSP00000501703.1:p.Phe174Leu
ENST00000674676.1:c.520T>C	ENSP00000502544.1:p.Phe174Leu
ENST00000674782.1:c.*722T>C	ENSP00000501683.1:n.*722T>C
ENST00000674937.1:c.760T>C	ENSP00000501823.1:p.Phe254Leu
ENST00000675322.1:c.520T>C	ENSP00000502235.1:p.Phe174Leu
ENST00000675675.1:c.520T>C	ENSP00000501793.1:p.Phe174Leu
ENST00000676178.1:c.*587T>C	ENSP00000502007.1:n.*587T>C
ENST00000676193.1:c.802T>C	ENSP00000502774.1:p.Phe268Leu
ENST00000331373.9:c.802T>C	ENSP00000331258.5:p.Phe268Leu
ENST00000614426.1:c.802T>C	ENSP00000478821.1:p.Phe268Leu
NM_001277971.1:c.802T>C	NP_001264900.1:p.Phe268Leu
NM_032237.4:c.802T>C	NP_115613.1:p.Phe268Leu
XM_011544668.1:c.802T>C	XP_011542970.1:p.Phe268Leu
XM_011544669.1:c.802T>C	XP_011542971.1:p.Phe268Leu
NM_032237.5:c.802T>C MANE Select	NP_115613.1:p.Phe268Leu
NM_001277971.2:c.802T>C	NP_001264900.1:p.Phe268Leu