Canonical Allele Identifier: CA371122797
Gene: POMK HGNC NCBI

Linked Data

gnomAD v4: 8-43122667-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43122667C>G , CM000670.2:g.43122667C>G GRCh38
NC_000008.10:g.42977810C>G , CM000670.1:g.42977810C>G GRCh37
NC_000008.9:g.43096967C>G NCBI36
NG_033235.1:g.34162C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331373.10:c.843C>G MANE Select ENSP00000331258.5:p.Asp281Glu
ENST00000614426.2:c.*639C>G ENSP00000478821.2:n.*639C>G
ENST00000674646.1:c.561C>G ENSP00000501703.1:p.Asp187Glu
ENST00000674676.1:c.561C>G ENSP00000502544.1:p.Asp187Glu
ENST00000674782.1:c.*763C>G ENSP00000501683.1:n.*763C>G
ENST00000674937.1:c.801C>G ENSP00000501823.1:p.Asp267Glu
ENST00000675322.1:c.561C>G ENSP00000502235.1:p.Asp187Glu
ENST00000675675.1:c.561C>G ENSP00000501793.1:p.Asp187Glu
ENST00000676178.1:c.*628C>G ENSP00000502007.1:n.*628C>G
ENST00000676193.1:c.843C>G ENSP00000502774.1:p.Asp281Glu
ENST00000331373.9:c.843C>G ENSP00000331258.5:p.Asp281Glu
ENST00000614426.1:c.843C>G ENSP00000478821.1:p.Asp281Glu
NM_001277971.1:c.843C>G NP_001264900.1:p.Asp281Glu
NM_032237.4:c.843C>G NP_115613.1:p.Asp281Glu
XM_011544668.1:c.843C>G XP_011542970.1:p.Asp281Glu
XM_011544669.1:c.843C>G XP_011542971.1:p.Asp281Glu
NM_032237.5:c.843C>G MANE Select NP_115613.1:p.Asp281Glu
NM_001277971.2:c.843C>G NP_001264900.1:p.Asp281Glu