Canonical Allele Identifier: CA1779736217
Gene: POMK HGNC NCBI

Linked Data

dbSNP Id: rs1811953496

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43122897A>G , CM000670.2:g.43122897A>G GRCh38
NC_000008.10:g.42978040A>G , CM000670.1:g.42978040A>G GRCh37
NC_000008.9:g.43097197A>G NCBI36
NG_033235.1:g.34392A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000331373.10:c.*20A>G MANE Select ENSP00000331258.5:n.*20A>G
ENST00000614426.2:c.*869A>G ENSP00000478821.2:n.*869A>G
ENST00000674646.1:c.791A>G ENSP00000501703.1:n.791A>G
ENST00000674676.1:c.791A>G ENSP00000502544.1:n.791A>G
ENST00000674782.1:c.*993A>G ENSP00000501683.1:n.*993A>G
ENST00000674937.1:c.*20A>G ENSP00000501823.1:n.*20A>G
ENST00000675322.1:c.791A>G ENSP00000502235.1:n.791A>G
ENST00000675675.1:c.791A>G ENSP00000501793.1:n.791A>G
ENST00000676178.1:c.*858A>G ENSP00000502007.1:n.*858A>G
ENST00000676193.1:c.*20A>G ENSP00000502774.1:n.*20A>G
ENST00000331373.9:c.*20A>G ENSP00000331258.5:n.*20A>G
ENST00000614426.1:c.*20A>G ENSP00000478821.1:n.*20A>G
NM_001277971.1:c.*20A>G NP_001264900.1:n.*20A>G
NM_032237.4:c.*20A>G NP_115613.1:n.*20A>G
XM_011544668.1:c.*20A>G XP_011542970.1:n.*20A>G
XM_011544669.1:c.*20A>G XP_011542971.1:n.*20A>G
NM_032237.5:c.*20A>G MANE Select NP_115613.1:n.*20A>G
NM_001277971.2:c.*20A>G NP_001264900.1:n.*20A>G