Canonical Allele Identifier: CA355076564

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514683T>G (hg19) ; chr3:g.169796895T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796895T>G , CM000665.2:g.169796895T>G	GRCh38
NC_000003.11:g.169514683T>G , CM000665.1:g.169514683T>G	GRCh37
NC_000003.10:g.170997377T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.758A>C MANE Select	ENSP00000414635.1:p.Glu253Ala
ENST00000446859.5:c.758A>C	ENSP00000414635.1:p.Glu253Ala
ENST00000522080.5:n.735A>C
ENST00000522329.1:n.7A>C
ENST00000522526.6:c.662A>C	ENSP00000429278.2:p.Glu221Ala
ENST00000522596.6:n.740A>C
ENST00000522830.5:c.575A>C	ENSP00000429593.1:p.Glu192Ala
ENST00000524054.5:n.606A>C
ENST00000524327.5:n.558A>C
ENST00000528597.1:c.5A>C	ENSP00000436883.1:p.Glu2Ala
ENST00000602774.1:n.144A>C
NM_001172779.1:c.758A>C	NP_001166250.1:p.Glu253Ala
NM_001172780.1:c.758A>C	NP_001166251.1:p.Glu253Ala
NM_153353.4:c.662A>C	NP_699184.2:p.Glu221Ala
XM_005247133.2:c.575A>C	XP_005247190.1:p.Glu192Ala
XM_006713508.2:c.704A>C	XP_006713571.1:p.Glu235Ala
XM_011512442.1:c.755A>C	XP_011510744.1:p.Glu252Ala
NM_001363888.1:c.575A>C	NP_001350817.1:p.Glu192Ala
XM_006713508.4:c.704A>C	XP_006713571.1:p.Glu235Ala
XM_011512442.2:c.755A>C	XP_011510744.1:p.Glu252Ala
XM_017005746.1:c.572A>C	XP_016861235.1:p.Glu191Ala
NM_001172779.2:c.758A>C MANE Select	NP_001166250.1:p.Glu253Ala
NM_001172780.2:c.758A>C	NP_001166251.1:p.Glu253Ala
NM_001363888.2:c.575A>C	NP_001350817.1:p.Glu192Ala
NM_001370608.1:c.572A>C	NP_001357537.1:p.Glu191Ala
NM_001370609.1:c.575A>C	NP_001357538.1:p.Glu192Ala
NM_153353.5:c.662A>C	NP_699184.2:p.Glu221Ala