Canonical Allele Identifier: CA460787570

Gene: POMK

Linked Data

• MyVariant Identifiers: chr8:g.42977462C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122319C>T , CM000670.2:g.43122319C>T	GRCh38
NC_000008.10:g.42977462C>T , CM000670.1:g.42977462C>T	GRCh37
NC_000008.9:g.43096619C>T	NCBI36
NG_033235.1:g.33814C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.495C>T MANE Select	ENSP00000331258.5:p.Asn165=
ENST00000614426.2:c.*291C>T	ENSP00000478821.2:n.*291C>T
ENST00000674646.1:c.213C>T	ENSP00000501703.1:p.Asn71=
ENST00000674676.1:c.213C>T	ENSP00000502544.1:p.Asn71=
ENST00000674782.1:c.*415C>T	ENSP00000501683.1:n.*415C>T
ENST00000674937.1:c.453C>T	ENSP00000501823.1:p.Asn151=
ENST00000675322.1:c.213C>T	ENSP00000502235.1:p.Asn71=
ENST00000675675.1:c.213C>T	ENSP00000501793.1:p.Asn71=
ENST00000676178.1:c.*280C>T	ENSP00000502007.1:n.*280C>T
ENST00000676193.1:c.495C>T	ENSP00000502774.1:p.Asn165=
ENST00000331373.9:c.495C>T	ENSP00000331258.5:p.Asn165=
ENST00000614426.1:c.495C>T	ENSP00000478821.1:p.Asn165=
NM_001277971.1:c.495C>T	NP_001264900.1:p.Asn165=
NM_032237.4:c.495C>T	NP_115613.1:p.Asn165=
XM_011544668.1:c.495C>T	XP_011542970.1:p.Asn165=
XM_011544669.1:c.495C>T	XP_011542971.1:p.Asn165=
NM_032237.5:c.495C>T MANE Select	NP_115613.1:p.Asn165=
NM_001277971.2:c.495C>T	NP_001264900.1:p.Asn165=