Canonical Allele Identifier: CA371122493

Gene: POMK

Linked Data

• gnomAD v4: 8-43122534-G-C
• MyVariant Identifiers: chr8:g.42977677G>C (hg19) ; chr8:g.43122534G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122534G>C , CM000670.2:g.43122534G>C	GRCh38
NC_000008.10:g.42977677G>C , CM000670.1:g.42977677G>C	GRCh37
NC_000008.9:g.43096834G>C	NCBI36
NG_033235.1:g.34029G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.710G>C MANE Select	ENSP00000331258.5:p.Ser237Thr
ENST00000614426.2:c.*506G>C	ENSP00000478821.2:n.*506G>C
ENST00000674646.1:c.428G>C	ENSP00000501703.1:p.Ser143Thr
ENST00000674676.1:c.428G>C	ENSP00000502544.1:p.Ser143Thr
ENST00000674782.1:c.*630G>C	ENSP00000501683.1:n.*630G>C
ENST00000674937.1:c.668G>C	ENSP00000501823.1:p.Ser223Thr
ENST00000675322.1:c.428G>C	ENSP00000502235.1:p.Ser143Thr
ENST00000675675.1:c.428G>C	ENSP00000501793.1:p.Ser143Thr
ENST00000676178.1:c.*495G>C	ENSP00000502007.1:n.*495G>C
ENST00000676193.1:c.710G>C	ENSP00000502774.1:p.Ser237Thr
ENST00000331373.9:c.710G>C	ENSP00000331258.5:p.Ser237Thr
ENST00000614426.1:c.710G>C	ENSP00000478821.1:p.Ser237Thr
NM_001277971.1:c.710G>C	NP_001264900.1:p.Ser237Thr
NM_032237.4:c.710G>C	NP_115613.1:p.Ser237Thr
XM_011544668.1:c.710G>C	XP_011542970.1:p.Ser237Thr
XM_011544669.1:c.710G>C	XP_011542971.1:p.Ser237Thr
NM_032237.5:c.710G>C MANE Select	NP_115613.1:p.Ser237Thr
NM_001277971.2:c.710G>C	NP_001264900.1:p.Ser237Thr