Canonical Allele Identifier: CA1419602170

Gene: LRRC34

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169800667T= , CM000665.2:g.169800667T=	GRCh38
NC_000003.11:g.169518455T= , CM000665.1:g.169518455T=	GRCh37
NC_000003.10:g.171001149T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001172779.2:c.745A= MANE Select	NP_001166250.1:p.Ser249=
ENST00000446859.7:c.745A= MANE Select	ENSP00000414635.1:p.Ser249=
NM_001172779.1:c.745A=	NP_001166250.1:p.Ser249=
NM_001172780.1:c.745A=	NP_001166251.1:p.Ser249=
NM_001172780.2:c.745A=	NP_001166251.1:p.Ser249=
NM_001363888.1:c.562A=	NP_001350817.1:p.Ser188=
NM_001363888.2:c.562A=	NP_001350817.1:p.Ser188=
NM_001370608.1:c.559A=	NP_001357537.1:p.Ser187=
NM_001370609.1:c.562A=	NP_001357538.1:p.Ser188=
NM_153353.4:c.657+3386A=	NP_699184.2:n.657+3386A=
NM_153353.5:c.657+3386A=	NP_699184.2:n.657+3386A=
ENST00000446859.5:c.745A=	ENSP00000414635.1:p.Ser249=
ENST00000522080.5:n.722A=
ENST00000522526.6:c.657+3386A=	ENSP00000429278.2:n.657+3386A=
ENST00000522596.6:n.727A=
ENST00000522830.5:c.562A=	ENSP00000429593.1:p.Ser188=
ENST00000524054.5:n.593A=
ENST00000524327.5:n.545A=
XM_005247133.2:c.562A=	XP_005247190.1:p.Ser188=
XM_006713508.2:c.691A=	XP_006713571.1:p.Ser231=
XM_006713508.4:c.691A=	XP_006713571.1:p.Ser231=
XM_011512442.1:c.742A=	XP_011510744.1:p.Ser248=
XM_011512442.2:c.742A=	XP_011510744.1:p.Ser248=
XM_017005746.1:c.559A=	XP_016861235.1:p.Ser187=