Canonical Allele Identifier: CA1779748202
Gene: POMK HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.43122781A= , CM000670.2:g.43122781A= GRCh38
NC_000008.10:g.42977924A= , CM000670.1:g.42977924A= GRCh37
NC_000008.9:g.43097081A= NCBI36
NG_033235.1:g.34276A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000331373.10:c.957A= MANE Select ENSP00000331258.5:p.Ser319=
ENST00000614426.2:c.*753A= ENSP00000478821.2:n.*753A=
ENST00000674646.1:c.675A= ENSP00000501703.1:p.Ser225=
ENST00000674676.1:c.675A= ENSP00000502544.1:p.Ser225=
ENST00000674782.1:c.*877A= ENSP00000501683.1:n.*877A=
ENST00000674937.1:c.915A= ENSP00000501823.1:p.Ser305=
ENST00000675322.1:c.675A= ENSP00000502235.1:p.Ser225=
ENST00000675675.1:c.675A= ENSP00000501793.1:p.Ser225=
ENST00000676178.1:c.*742A= ENSP00000502007.1:n.*742A=
ENST00000676193.1:c.957A= ENSP00000502774.1:p.Ser319=
ENST00000331373.9:c.957A= ENSP00000331258.5:p.Ser319=
ENST00000614426.1:c.957A= ENSP00000478821.1:p.Ser319=
NM_001277971.1:c.957A= NP_001264900.1:p.Ser319=
NM_032237.4:c.957A= NP_115613.1:p.Ser319=
XM_011544668.1:c.957A= XP_011542970.1:p.Ser319=
XM_011544669.1:c.957A= XP_011542971.1:p.Ser319=
NM_032237.5:c.957A= MANE Select NP_115613.1:p.Ser319=
NM_001277971.2:c.957A= NP_001264900.1:p.Ser319=