Canonical Allele Identifier: CA1419595379

Gene: LRRC34

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796797A= , CM000665.2:g.169796797A=	GRCh38
NC_000003.11:g.169514585A= , CM000665.1:g.169514585A=	GRCh37
NC_000003.10:g.170997279A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.856T= MANE Select	ENSP00000414635.1:p.Leu286=
ENST00000446859.5:c.856T=	ENSP00000414635.1:p.Leu286=
ENST00000522080.5:n.833T=
ENST00000522329.1:n.105T=
ENST00000522526.6:c.760T=	ENSP00000429278.2:p.Leu254=
ENST00000522596.6:n.838T=
ENST00000522830.5:c.673T=	ENSP00000429593.1:p.Leu225=
ENST00000524054.5:n.704T=
ENST00000524327.5:n.656T=
ENST00000528597.1:c.103T=	ENSP00000436883.1:p.Leu35=
ENST00000602774.1:n.242T=
NM_001172779.1:c.856T=	NP_001166250.1:p.Leu286=
NM_001172780.1:c.856T=	NP_001166251.1:p.Leu286=
NM_153353.4:c.760T=	NP_699184.2:p.Leu254=
XM_005247133.2:c.673T=	XP_005247190.1:p.Leu225=
XM_006713508.2:c.802T=	XP_006713571.1:p.Leu268=
XM_011512442.1:c.853T=	XP_011510744.1:p.Leu285=
NM_001363888.1:c.673T=	NP_001350817.1:p.Leu225=
XM_006713508.4:c.802T=	XP_006713571.1:p.Leu268=
XM_011512442.2:c.853T=	XP_011510744.1:p.Leu285=
XM_017005746.1:c.670T=	XP_016861235.1:p.Leu224=
NM_001172779.2:c.856T= MANE Select	NP_001166250.1:p.Leu286=
NM_001172780.2:c.856T=	NP_001166251.1:p.Leu286=
NM_001363888.2:c.673T=	NP_001350817.1:p.Leu225=
NM_001370608.1:c.670T=	NP_001357537.1:p.Leu224=
NM_001370609.1:c.673T=	NP_001357538.1:p.Leu225=
NM_153353.5:c.760T=	NP_699184.2:p.Leu254=