Canonical Allele Identifier: CA4736310

Gene: POMK

Linked Data

• ClinVar Variation Id: 761753
• ClinVar RCV Id: RCV001433249 ; RCV003913185
• dbSNP Id: rs766337800
• ExAC: 8:42977555 T / C
• gnomAD v2: 8-42977555-T-C
• gnomAD v3: 8-43122412-T-C
• gnomAD v4: 8-43122412-T-C
• MyVariant Identifiers: chr8:g.42977555T>C (hg19) ; chr8:g.43122412T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122412T>C , CM000670.2:g.43122412T>C	GRCh38
NC_000008.10:g.42977555T>C , CM000670.1:g.42977555T>C	GRCh37
NC_000008.9:g.43096712T>C	NCBI36
NG_033235.1:g.33907T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.588T>C MANE Select	ENSP00000331258.5:p.Pro196=
ENST00000614426.2:c.*384T>C	ENSP00000478821.2:n.*384T>C
ENST00000674646.1:c.306T>C	ENSP00000501703.1:p.Pro102=
ENST00000674676.1:c.306T>C	ENSP00000502544.1:p.Pro102=
ENST00000674782.1:c.*508T>C	ENSP00000501683.1:n.*508T>C
ENST00000674937.1:c.546T>C	ENSP00000501823.1:p.Pro182=
ENST00000675322.1:c.306T>C	ENSP00000502235.1:p.Pro102=
ENST00000675675.1:c.306T>C	ENSP00000501793.1:p.Pro102=
ENST00000676178.1:c.*373T>C	ENSP00000502007.1:n.*373T>C
ENST00000676193.1:c.588T>C	ENSP00000502774.1:p.Pro196=
ENST00000331373.9:c.588T>C	ENSP00000331258.5:p.Pro196=
ENST00000614426.1:c.588T>C	ENSP00000478821.1:p.Pro196=
NM_001277971.1:c.588T>C	NP_001264900.1:p.Pro196=
NM_032237.4:c.588T>C	NP_115613.1:p.Pro196=
XM_011544668.1:c.588T>C	XP_011542970.1:p.Pro196=
XM_011544669.1:c.588T>C	XP_011542971.1:p.Pro196=
NM_032237.5:c.588T>C MANE Select	NP_115613.1:p.Pro196=
NM_001277971.2:c.588T>C	NP_001264900.1:p.Pro196=