Canonical Allele Identifier: CA355077229

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169518466G>C (hg19) ; chr3:g.169800678G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169800678G>C , CM000665.2:g.169800678G>C	GRCh38
NC_000003.11:g.169518466G>C , CM000665.1:g.169518466G>C	GRCh37
NC_000003.10:g.171001160G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.734C>G MANE Select	ENSP00000414635.1:p.Pro245Arg
ENST00000446859.5:c.734C>G	ENSP00000414635.1:p.Pro245Arg
ENST00000522080.5:n.711C>G
ENST00000522526.6:c.657+3375C>G	ENSP00000429278.2:n.657+3375C>G
ENST00000522596.6:n.716C>G
ENST00000522830.5:c.551C>G	ENSP00000429593.1:p.Pro184Arg
ENST00000524054.5:n.582C>G
ENST00000524327.5:n.534C>G
NM_001172779.1:c.734C>G	NP_001166250.1:p.Pro245Arg
NM_001172780.1:c.734C>G	NP_001166251.1:p.Pro245Arg
NM_153353.4:c.657+3375C>G	NP_699184.2:n.657+3375C>G
XM_005247133.2:c.551C>G	XP_005247190.1:p.Pro184Arg
XM_006713508.2:c.680C>G	XP_006713571.1:p.Pro227Arg
XM_011512442.1:c.731C>G	XP_011510744.1:p.Pro244Arg
NM_001363888.1:c.551C>G	NP_001350817.1:p.Pro184Arg
XM_006713508.4:c.680C>G	XP_006713571.1:p.Pro227Arg
XM_011512442.2:c.731C>G	XP_011510744.1:p.Pro244Arg
XM_017005746.1:c.548C>G	XP_016861235.1:p.Pro183Arg
NM_001172779.2:c.734C>G MANE Select	NP_001166250.1:p.Pro245Arg
NM_001172780.2:c.734C>G	NP_001166251.1:p.Pro245Arg
NM_001363888.2:c.551C>G	NP_001350817.1:p.Pro184Arg
NM_001370608.1:c.548C>G	NP_001357537.1:p.Pro183Arg
NM_001370609.1:c.551C>G	NP_001357538.1:p.Pro184Arg
NM_153353.5:c.657+3375C>G	NP_699184.2:n.657+3375C>G