Canonical Allele Identifier: CA436763708

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514661G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796873G>C , CM000665.2:g.169796873G>C	GRCh38
NC_000003.11:g.169514661G>C , CM000665.1:g.169514661G>C	GRCh37
NC_000003.10:g.170997355G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.780C>G MANE Select	ENSP00000414635.1:p.Arg260=
ENST00000446859.5:c.780C>G	ENSP00000414635.1:p.Arg260=
ENST00000522080.5:n.757C>G
ENST00000522329.1:n.29C>G
ENST00000522526.6:c.684C>G	ENSP00000429278.2:p.Arg228=
ENST00000522596.6:n.762C>G
ENST00000522830.5:c.597C>G	ENSP00000429593.1:p.Arg199=
ENST00000524054.5:n.628C>G
ENST00000524327.5:n.580C>G
ENST00000528597.1:c.27C>G	ENSP00000436883.1:p.Arg9=
ENST00000602774.1:n.166C>G
NM_001172779.1:c.780C>G	NP_001166250.1:p.Arg260=
NM_001172780.1:c.780C>G	NP_001166251.1:p.Arg260=
NM_153353.4:c.684C>G	NP_699184.2:p.Arg228=
XM_005247133.2:c.597C>G	XP_005247190.1:p.Arg199=
XM_006713508.2:c.726C>G	XP_006713571.1:p.Arg242=
XM_011512442.1:c.777C>G	XP_011510744.1:p.Arg259=
NM_001363888.1:c.597C>G	NP_001350817.1:p.Arg199=
XM_006713508.4:c.726C>G	XP_006713571.1:p.Arg242=
XM_011512442.2:c.777C>G	XP_011510744.1:p.Arg259=
XM_017005746.1:c.594C>G	XP_016861235.1:p.Arg198=
NM_001172779.2:c.780C>G MANE Select	NP_001166250.1:p.Arg260=
NM_001172780.2:c.780C>G	NP_001166251.1:p.Arg260=
NM_001363888.2:c.597C>G	NP_001350817.1:p.Arg199=
NM_001370608.1:c.594C>G	NP_001357537.1:p.Arg198=
NM_001370609.1:c.597C>G	NP_001357538.1:p.Arg199=
NM_153353.5:c.684C>G	NP_699184.2:p.Arg228=