Canonical Allele Identifier: CA436763681

Gene: LRRC34

Linked Data

• COSMIC: COSM5658439 ; COSM5658440
• MyVariant Identifiers: chr3:g.169514595A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796807A>G , CM000665.2:g.169796807A>G	GRCh38
NC_000003.11:g.169514595A>G , CM000665.1:g.169514595A>G	GRCh37
NC_000003.10:g.170997289A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.846T>C MANE Select	ENSP00000414635.1:p.Gly282=
ENST00000446859.5:c.846T>C	ENSP00000414635.1:p.Gly282=
ENST00000522080.5:n.823T>C
ENST00000522329.1:n.95T>C
ENST00000522526.6:c.750T>C	ENSP00000429278.2:p.Gly250=
ENST00000522596.6:n.828T>C
ENST00000522830.5:c.663T>C	ENSP00000429593.1:p.Gly221=
ENST00000524054.5:n.694T>C
ENST00000524327.5:n.646T>C
ENST00000528597.1:c.93T>C	ENSP00000436883.1:p.Gly31=
ENST00000602774.1:n.232T>C
NM_001172779.1:c.846T>C	NP_001166250.1:p.Gly282=
NM_001172780.1:c.846T>C	NP_001166251.1:p.Gly282=
NM_153353.4:c.750T>C	NP_699184.2:p.Gly250=
XM_005247133.2:c.663T>C	XP_005247190.1:p.Gly221=
XM_006713508.2:c.792T>C	XP_006713571.1:p.Gly264=
XM_011512442.1:c.843T>C	XP_011510744.1:p.Gly281=
NM_001363888.1:c.663T>C	NP_001350817.1:p.Gly221=
XM_006713508.4:c.792T>C	XP_006713571.1:p.Gly264=
XM_011512442.2:c.843T>C	XP_011510744.1:p.Gly281=
XM_017005746.1:c.660T>C	XP_016861235.1:p.Gly220=
NM_001172779.2:c.846T>C MANE Select	NP_001166250.1:p.Gly282=
NM_001172780.2:c.846T>C	NP_001166251.1:p.Gly282=
NM_001363888.2:c.663T>C	NP_001350817.1:p.Gly221=
NM_001370608.1:c.660T>C	NP_001357537.1:p.Gly220=
NM_001370609.1:c.663T>C	NP_001357538.1:p.Gly221=
NM_153353.5:c.750T>C	NP_699184.2:p.Gly250=