Canonical Allele Identifier: CA1419595147

Gene: LRRC34

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796742T= , CM000665.2:g.169796742T=	GRCh38
NC_000003.11:g.169514530T= , CM000665.1:g.169514530T=	GRCh37
NC_000003.10:g.170997224T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.908+3A= MANE Select	ENSP00000414635.1:n.908+3A=
ENST00000446859.5:c.908+3A=	ENSP00000414635.1:n.908+3A=
ENST00000522080.5:n.885+3A=
ENST00000522329.1:n.157+3A=
ENST00000522526.6:c.812+3A=	ENSP00000429278.2:n.812+3A=
ENST00000522596.6:n.890+3A=
ENST00000522830.5:c.725+3A=	ENSP00000429593.1:n.725+3A=
ENST00000524327.5:n.708+3A=
ENST00000528597.1:c.155+3A=	ENSP00000436883.1:n.155+3A=
ENST00000602774.1:n.297A=
NM_001172779.1:c.908+3A=	NP_001166250.1:n.908+3A=
NM_001172780.1:c.908+3A=	NP_001166251.1:n.908+3A=
NM_153353.4:c.812+3A=	NP_699184.2:n.812+3A=
XM_005247133.2:c.725+3A=	XP_005247190.1:n.725+3A=
XM_006713508.2:c.854+3A=	XP_006713571.1:n.854+3A=
XM_011512442.1:c.905+3A=	XP_011510744.1:n.905+3A=
NM_001363888.1:c.725+3A=	NP_001350817.1:n.725+3A=
XM_006713508.4:c.854+3A=	XP_006713571.1:n.854+3A=
XM_011512442.2:c.905+3A=	XP_011510744.1:n.905+3A=
XM_017005746.1:c.722+3A=	XP_016861235.1:n.722+3A=
NM_001172779.2:c.908+3A= MANE Select	NP_001166250.1:n.908+3A=
NM_001172780.2:c.908+3A=	NP_001166251.1:n.908+3A=
NM_001363888.2:c.725+3A=	NP_001350817.1:n.725+3A=
NM_001370608.1:c.722+3A=	NP_001357537.1:n.722+3A=
NM_001370609.1:c.725+3A=	NP_001357538.1:n.725+3A=
NM_153353.5:c.812+3A=	NP_699184.2:n.812+3A=