Canonical Allele Identifier: CA1779747526
Gene: POMK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43122487C= , CM000670.2:g.43122487C= GRCh38
NC_000008.10:g.42977630C= , CM000670.1:g.42977630C= GRCh37
NC_000008.9:g.43096787C= NCBI36
NG_033235.1:g.33982C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331373.10:c.663C= MANE Select ENSP00000331258.5:p.Phe221=
ENST00000614426.2:c.*459C= ENSP00000478821.2:n.*459C=
ENST00000674646.1:c.381C= ENSP00000501703.1:p.Phe127=
ENST00000674676.1:c.381C= ENSP00000502544.1:p.Phe127=
ENST00000674782.1:c.*583C= ENSP00000501683.1:n.*583C=
ENST00000674937.1:c.621C= ENSP00000501823.1:p.Phe207=
ENST00000675322.1:c.381C= ENSP00000502235.1:p.Phe127=
ENST00000675675.1:c.381C= ENSP00000501793.1:p.Phe127=
ENST00000676178.1:c.*448C= ENSP00000502007.1:n.*448C=
ENST00000676193.1:c.663C= ENSP00000502774.1:p.Phe221=
ENST00000331373.9:c.663C= ENSP00000331258.5:p.Phe221=
ENST00000614426.1:c.663C= ENSP00000478821.1:p.Phe221=
NM_001277971.1:c.663C= NP_001264900.1:p.Phe221=
NM_032237.4:c.663C= NP_115613.1:p.Phe221=
XM_011544668.1:c.663C= XP_011542970.1:p.Phe221=
XM_011544669.1:c.663C= XP_011542971.1:p.Phe221=
NM_032237.5:c.663C= MANE Select NP_115613.1:p.Phe221=
NM_001277971.2:c.663C= NP_001264900.1:p.Phe221=