Canonical Allele Identifier: CA7214948

Gene: TMEM30B PRKCH

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.61280958C>G , CM000676.2:g.61280958C>G	GRCh38
NC_000014.8:g.61747676C>G , CM000676.1:g.61747676C>G	GRCh37
NC_000014.7:g.60817429C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000555868.2:c.190G>C (TMEM30B) MANE Select	ENSP00000450842.1:p.Glu64Gln
ENST00000554497.1:n.435G>C (TMEM30B)
ENST00000555185.5:c.-19+93290C>G (PRKCH)	ENSP00000451871.1:n.-19+93290C>G
ENST00000555542.5:c.-471C>G (PRKCH)	ENSP00000451789.1:n.-471C>G
ENST00000555868.1:c.190G>C (TMEM30B)	ENSP00000450842.1:p.Glu64Gln
ENST00000556778.5:c.-57+93290C>G (PRKCH)	ENSP00000452055.1:n.-57+93290C>G
ENST00000557163.1:n.180-3G>C (TMEM30B)
ENST00000557294.5:c.-108-41036C>G (PRKCH)	ENSP00000452129.1:n.-108-41036C>G
NM_001017970.2:c.190G>C (TMEM30B)	NP_001017970.1:p.Glu64Gln
XM_017021458.1:c.-471C>G (PRKCH)	XP_016876947.1:n.-471C>G
XM_024449661.1:c.-121+93290C>G (PRKCH)	XP_024305429.1:n.-121+93290C>G
NM_001017970.3:c.190G>C (TMEM30B) MANE Select	NP_001017970.1:p.Glu64Gln