Canonical Allele Identifier: CA436764425

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169518459C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169800671C>A , CM000665.2:g.169800671C>A	GRCh38
NC_000003.11:g.169518459C>A , CM000665.1:g.169518459C>A	GRCh37
NC_000003.10:g.171001153C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.741G>T MANE Select	ENSP00000414635.1:p.Leu247=
ENST00000446859.5:c.741G>T	ENSP00000414635.1:p.Leu247=
ENST00000522080.5:n.718G>T
ENST00000522526.6:c.657+3382G>T	ENSP00000429278.2:n.657+3382G>T
ENST00000522596.6:n.723G>T
ENST00000522830.5:c.558G>T	ENSP00000429593.1:p.Leu186=
ENST00000524054.5:n.589G>T
ENST00000524327.5:n.541G>T
NM_001172779.1:c.741G>T	NP_001166250.1:p.Leu247=
NM_001172780.1:c.741G>T	NP_001166251.1:p.Leu247=
NM_153353.4:c.657+3382G>T	NP_699184.2:n.657+3382G>T
XM_005247133.2:c.558G>T	XP_005247190.1:p.Leu186=
XM_006713508.2:c.687G>T	XP_006713571.1:p.Leu229=
XM_011512442.1:c.738G>T	XP_011510744.1:p.Leu246=
NM_001363888.1:c.558G>T	NP_001350817.1:p.Leu186=
XM_006713508.4:c.687G>T	XP_006713571.1:p.Leu229=
XM_011512442.2:c.738G>T	XP_011510744.1:p.Leu246=
XM_017005746.1:c.555G>T	XP_016861235.1:p.Leu185=
NM_001172779.2:c.741G>T MANE Select	NP_001166250.1:p.Leu247=
NM_001172780.2:c.741G>T	NP_001166251.1:p.Leu247=
NM_001363888.2:c.558G>T	NP_001350817.1:p.Leu186=
NM_001370608.1:c.555G>T	NP_001357537.1:p.Leu185=
NM_001370609.1:c.558G>T	NP_001357538.1:p.Leu186=
NM_153353.5:c.657+3382G>T	NP_699184.2:n.657+3382G>T