Canonical Allele Identifier: CA1779747762
Gene: POMK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43122636A= , CM000670.2:g.43122636A= GRCh38
NC_000008.10:g.42977779A= , CM000670.1:g.42977779A= GRCh37
NC_000008.9:g.43096936A= NCBI36
NG_033235.1:g.34131A=

Transcript Alleles

HGVS Amino-acid change
ENST00000331373.10:c.812A= MANE Select ENSP00000331258.5:p.Asp271=
ENST00000614426.2:c.*608A= ENSP00000478821.2:n.*608A=
ENST00000674646.1:c.530A= ENSP00000501703.1:p.Asp177=
ENST00000674676.1:c.530A= ENSP00000502544.1:p.Asp177=
ENST00000674782.1:c.*732A= ENSP00000501683.1:n.*732A=
ENST00000674937.1:c.770A= ENSP00000501823.1:p.Asp257=
ENST00000675322.1:c.530A= ENSP00000502235.1:p.Asp177=
ENST00000675675.1:c.530A= ENSP00000501793.1:p.Asp177=
ENST00000676178.1:c.*597A= ENSP00000502007.1:n.*597A=
ENST00000676193.1:c.812A= ENSP00000502774.1:p.Asp271=
ENST00000331373.9:c.812A= ENSP00000331258.5:p.Asp271=
ENST00000614426.1:c.812A= ENSP00000478821.1:p.Asp271=
NM_001277971.1:c.812A= NP_001264900.1:p.Asp271=
NM_032237.4:c.812A= NP_115613.1:p.Asp271=
XM_011544668.1:c.812A= XP_011542970.1:p.Asp271=
XM_011544669.1:c.812A= XP_011542971.1:p.Asp271=
NM_032237.5:c.812A= MANE Select NP_115613.1:p.Asp271=
NM_001277971.2:c.812A= NP_001264900.1:p.Asp271=