Canonical Allele Identifier: CA1419595275

Gene: LRRC34

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796767G= , CM000665.2:g.169796767G=	GRCh38
NC_000003.11:g.169514555G= , CM000665.1:g.169514555G=	GRCh37
NC_000003.10:g.170997249G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.886C= MANE Select	ENSP00000414635.1:p.Leu296=
ENST00000446859.5:c.886C=	ENSP00000414635.1:p.Leu296=
ENST00000522080.5:n.863C=
ENST00000522329.1:n.135C=
ENST00000522526.6:c.790C=	ENSP00000429278.2:p.Leu264=
ENST00000522596.6:n.868C=
ENST00000522830.5:c.703C=	ENSP00000429593.1:p.Leu235=
ENST00000524054.5:n.734C=
ENST00000524327.5:n.686C=
ENST00000528597.1:c.133C=	ENSP00000436883.1:p.Leu45=
ENST00000602774.1:n.272C=
NM_001172779.1:c.886C=	NP_001166250.1:p.Leu296=
NM_001172780.1:c.886C=	NP_001166251.1:p.Leu296=
NM_153353.4:c.790C=	NP_699184.2:p.Leu264=
XM_005247133.2:c.703C=	XP_005247190.1:p.Leu235=
XM_006713508.2:c.832C=	XP_006713571.1:p.Leu278=
XM_011512442.1:c.883C=	XP_011510744.1:p.Leu295=
NM_001363888.1:c.703C=	NP_001350817.1:p.Leu235=
XM_006713508.4:c.832C=	XP_006713571.1:p.Leu278=
XM_011512442.2:c.883C=	XP_011510744.1:p.Leu295=
XM_017005746.1:c.700C=	XP_016861235.1:p.Leu234=
NM_001172779.2:c.886C= MANE Select	NP_001166250.1:p.Leu296=
NM_001172780.2:c.886C=	NP_001166251.1:p.Leu296=
NM_001363888.2:c.703C=	NP_001350817.1:p.Leu235=
NM_001370608.1:c.700C=	NP_001357537.1:p.Leu234=
NM_001370609.1:c.703C=	NP_001357538.1:p.Leu235=
NM_153353.5:c.790C=	NP_699184.2:p.Leu264=