Canonical Allele Identifier: CA1419595469

Gene: LRRC34

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796811C= , CM000665.2:g.169796811C=	GRCh38
NC_000003.11:g.169514599C= , CM000665.1:g.169514599C=	GRCh37
NC_000003.10:g.170997293C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.842G= MANE Select	ENSP00000414635.1:p.Ser281=
ENST00000446859.5:c.842G=	ENSP00000414635.1:p.Ser281=
ENST00000522080.5:n.819G=
ENST00000522329.1:n.91G=
ENST00000522526.6:c.746G=	ENSP00000429278.2:p.Ser249=
ENST00000522596.6:n.824G=
ENST00000522830.5:c.659G=	ENSP00000429593.1:p.Ser220=
ENST00000524054.5:n.690G=
ENST00000524327.5:n.642G=
ENST00000528597.1:c.89G=	ENSP00000436883.1:p.Ser30=
ENST00000602774.1:n.228G=
NM_001172779.1:c.842G=	NP_001166250.1:p.Ser281=
NM_001172780.1:c.842G=	NP_001166251.1:p.Ser281=
NM_153353.4:c.746G=	NP_699184.2:p.Ser249=
XM_005247133.2:c.659G=	XP_005247190.1:p.Ser220=
XM_006713508.2:c.788G=	XP_006713571.1:p.Ser263=
XM_011512442.1:c.839G=	XP_011510744.1:p.Ser280=
NM_001363888.1:c.659G=	NP_001350817.1:p.Ser220=
XM_006713508.4:c.788G=	XP_006713571.1:p.Ser263=
XM_011512442.2:c.839G=	XP_011510744.1:p.Ser280=
XM_017005746.1:c.656G=	XP_016861235.1:p.Ser219=
NM_001172779.2:c.842G= MANE Select	NP_001166250.1:p.Ser281=
NM_001172780.2:c.842G=	NP_001166251.1:p.Ser281=
NM_001363888.2:c.659G=	NP_001350817.1:p.Ser220=
NM_001370608.1:c.656G=	NP_001357537.1:p.Ser219=
NM_001370609.1:c.659G=	NP_001357538.1:p.Ser220=
NM_153353.5:c.746G=	NP_699184.2:p.Ser249=