Canonical Allele Identifier: CA460787374
Gene: POMK HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.42977684G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43122541G>C , CM000670.2:g.43122541G>C GRCh38
NC_000008.10:g.42977684G>C , CM000670.1:g.42977684G>C GRCh37
NC_000008.9:g.43096841G>C NCBI36
NG_033235.1:g.34036G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000331373.10:c.717G>C MANE Select ENSP00000331258.5:p.Gly239=
ENST00000614426.2:c.*513G>C ENSP00000478821.2:n.*513G>C
ENST00000674646.1:c.435G>C ENSP00000501703.1:p.Gly145=
ENST00000674676.1:c.435G>C ENSP00000502544.1:p.Gly145=
ENST00000674782.1:c.*637G>C ENSP00000501683.1:n.*637G>C
ENST00000674937.1:c.675G>C ENSP00000501823.1:p.Gly225=
ENST00000675322.1:c.435G>C ENSP00000502235.1:p.Gly145=
ENST00000675675.1:c.435G>C ENSP00000501793.1:p.Gly145=
ENST00000676178.1:c.*502G>C ENSP00000502007.1:n.*502G>C
ENST00000676193.1:c.717G>C ENSP00000502774.1:p.Gly239=
ENST00000331373.9:c.717G>C ENSP00000331258.5:p.Gly239=
ENST00000614426.1:c.717G>C ENSP00000478821.1:p.Gly239=
NM_001277971.1:c.717G>C NP_001264900.1:p.Gly239=
NM_032237.4:c.717G>C NP_115613.1:p.Gly239=
XM_011544668.1:c.717G>C XP_011542970.1:p.Gly239=
XM_011544669.1:c.717G>C XP_011542971.1:p.Gly239=
NM_032237.5:c.717G>C MANE Select NP_115613.1:p.Gly239=
NM_001277971.2:c.717G>C NP_001264900.1:p.Gly239=