Canonical Allele Identifier: CA1419595283

Gene: LRRC34

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796774G= , CM000665.2:g.169796774G=	GRCh38
NC_000003.11:g.169514562G= , CM000665.1:g.169514562G=	GRCh37
NC_000003.10:g.170997256G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.879C= MANE Select	ENSP00000414635.1:p.Asn293=
ENST00000446859.5:c.879C=	ENSP00000414635.1:p.Asn293=
ENST00000522080.5:n.856C=
ENST00000522329.1:n.128C=
ENST00000522526.6:c.783C=	ENSP00000429278.2:p.Asn261=
ENST00000522596.6:n.861C=
ENST00000522830.5:c.696C=	ENSP00000429593.1:p.Asn232=
ENST00000524054.5:n.727C=
ENST00000524327.5:n.679C=
ENST00000528597.1:c.126C=	ENSP00000436883.1:p.Asn42=
ENST00000602774.1:n.265C=
NM_001172779.1:c.879C=	NP_001166250.1:p.Asn293=
NM_001172780.1:c.879C=	NP_001166251.1:p.Asn293=
NM_153353.4:c.783C=	NP_699184.2:p.Asn261=
XM_005247133.2:c.696C=	XP_005247190.1:p.Asn232=
XM_006713508.2:c.825C=	XP_006713571.1:p.Asn275=
XM_011512442.1:c.876C=	XP_011510744.1:p.Asn292=
NM_001363888.1:c.696C=	NP_001350817.1:p.Asn232=
XM_006713508.4:c.825C=	XP_006713571.1:p.Asn275=
XM_011512442.2:c.876C=	XP_011510744.1:p.Asn292=
XM_017005746.1:c.693C=	XP_016861235.1:p.Asn231=
NM_001172779.2:c.879C= MANE Select	NP_001166250.1:p.Asn293=
NM_001172780.2:c.879C=	NP_001166251.1:p.Asn293=
NM_001363888.2:c.696C=	NP_001350817.1:p.Asn232=
NM_001370608.1:c.693C=	NP_001357537.1:p.Asn231=
NM_001370609.1:c.696C=	NP_001357538.1:p.Asn232=
NM_153353.5:c.783C=	NP_699184.2:p.Asn261=