Canonical Allele Identifier: CA460787478

Gene: POMK

Linked Data

• MyVariant Identifiers: chr8:g.42977735A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122592A>C , CM000670.2:g.43122592A>C	GRCh38
NC_000008.10:g.42977735A>C , CM000670.1:g.42977735A>C	GRCh37
NC_000008.9:g.43096892A>C	NCBI36
NG_033235.1:g.34087A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.768A>C MANE Select	ENSP00000331258.5:p.Pro256=
ENST00000614426.2:c.*564A>C	ENSP00000478821.2:n.*564A>C
ENST00000674646.1:c.486A>C	ENSP00000501703.1:p.Pro162=
ENST00000674676.1:c.486A>C	ENSP00000502544.1:p.Pro162=
ENST00000674782.1:c.*688A>C	ENSP00000501683.1:n.*688A>C
ENST00000674937.1:c.726A>C	ENSP00000501823.1:p.Pro242=
ENST00000675322.1:c.486A>C	ENSP00000502235.1:p.Pro162=
ENST00000675675.1:c.486A>C	ENSP00000501793.1:p.Pro162=
ENST00000676178.1:c.*553A>C	ENSP00000502007.1:n.*553A>C
ENST00000676193.1:c.768A>C	ENSP00000502774.1:p.Pro256=
ENST00000331373.9:c.768A>C	ENSP00000331258.5:p.Pro256=
ENST00000614426.1:c.768A>C	ENSP00000478821.1:p.Pro256=
NM_001277971.1:c.768A>C	NP_001264900.1:p.Pro256=
NM_032237.4:c.768A>C	NP_115613.1:p.Pro256=
XM_011544668.1:c.768A>C	XP_011542970.1:p.Pro256=
XM_011544669.1:c.768A>C	XP_011542971.1:p.Pro256=
NM_032237.5:c.768A>C MANE Select	NP_115613.1:p.Pro256=
NM_001277971.2:c.768A>C	NP_001264900.1:p.Pro256=