Canonical Allele Identifier: CA371122958

Gene: POMK

Linked Data

• MyVariant Identifiers: chr8:g.42977884T>C (hg19) ; chr8:g.43122741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122741T>C , CM000670.2:g.43122741T>C	GRCh38
NC_000008.10:g.42977884T>C , CM000670.1:g.42977884T>C	GRCh37
NC_000008.9:g.43097041T>C	NCBI36
NG_033235.1:g.34236T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000331373.10:c.917T>C MANE Select	ENSP00000331258.5:p.Leu306Ser
ENST00000614426.2:c.*713T>C	ENSP00000478821.2:n.*713T>C
ENST00000674646.1:c.635T>C	ENSP00000501703.1:p.Leu212Ser
ENST00000674676.1:c.635T>C	ENSP00000502544.1:p.Leu212Ser
ENST00000674782.1:c.*837T>C	ENSP00000501683.1:n.*837T>C
ENST00000674937.1:c.875T>C	ENSP00000501823.1:p.Leu292Ser
ENST00000675322.1:c.635T>C	ENSP00000502235.1:p.Leu212Ser
ENST00000675675.1:c.635T>C	ENSP00000501793.1:p.Leu212Ser
ENST00000676178.1:c.*702T>C	ENSP00000502007.1:n.*702T>C
ENST00000676193.1:c.917T>C	ENSP00000502774.1:p.Leu306Ser
ENST00000331373.9:c.917T>C	ENSP00000331258.5:p.Leu306Ser
ENST00000614426.1:c.917T>C	ENSP00000478821.1:p.Leu306Ser
NM_001277971.1:c.917T>C	NP_001264900.1:p.Leu306Ser
NM_032237.4:c.917T>C	NP_115613.1:p.Leu306Ser
XM_011544668.1:c.917T>C	XP_011542970.1:p.Leu306Ser
XM_011544669.1:c.917T>C	XP_011542971.1:p.Leu306Ser
NM_032237.5:c.917T>C MANE Select	NP_115613.1:p.Leu306Ser
NM_001277971.2:c.917T>C	NP_001264900.1:p.Leu306Ser