Canonical Allele Identifier: CA371122049

Gene: POMK

Linked Data

• MyVariant Identifiers: chr8:g.42977472T>G (hg19) ; chr8:g.43122329T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.43122329T>G , CM000670.2:g.43122329T>G	GRCh38
NC_000008.10:g.42977472T>G , CM000670.1:g.42977472T>G	GRCh37
NC_000008.9:g.43096629T>G	NCBI36
NG_033235.1:g.33824T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331373.10:c.505T>G MANE Select	ENSP00000331258.5:p.Tyr169Asp
ENST00000614426.2:c.*301T>G	ENSP00000478821.2:n.*301T>G
ENST00000674646.1:c.223T>G	ENSP00000501703.1:p.Tyr75Asp
ENST00000674676.1:c.223T>G	ENSP00000502544.1:p.Tyr75Asp
ENST00000674782.1:c.*425T>G	ENSP00000501683.1:n.*425T>G
ENST00000674937.1:c.463T>G	ENSP00000501823.1:p.Tyr155Asp
ENST00000675322.1:c.223T>G	ENSP00000502235.1:p.Tyr75Asp
ENST00000675675.1:c.223T>G	ENSP00000501793.1:p.Tyr75Asp
ENST00000676178.1:c.*290T>G	ENSP00000502007.1:n.*290T>G
ENST00000676193.1:c.505T>G	ENSP00000502774.1:p.Tyr169Asp
ENST00000331373.9:c.505T>G	ENSP00000331258.5:p.Tyr169Asp
ENST00000614426.1:c.505T>G	ENSP00000478821.1:p.Tyr169Asp
NM_001277971.1:c.505T>G	NP_001264900.1:p.Tyr169Asp
NM_032237.4:c.505T>G	NP_115613.1:p.Tyr169Asp
XM_011544668.1:c.505T>G	XP_011542970.1:p.Tyr169Asp
XM_011544669.1:c.505T>G	XP_011542971.1:p.Tyr169Asp
NM_032237.5:c.505T>G MANE Select	NP_115613.1:p.Tyr169Asp
NM_001277971.2:c.505T>G	NP_001264900.1:p.Tyr169Asp