Canonical Allele Identifier: CA547940016

Gene: LRRC34

Linked Data

• dbSNP Id: rs1417271469
• gnomAD v2: 3-169514486-T-C
• MyVariant Identifiers: chr3:g.169514486T>C (hg19) ; chr3:g.169796698T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796698T>C , CM000665.2:g.169796698T>C	GRCh38
NC_000003.11:g.169514486T>C , CM000665.1:g.169514486T>C	GRCh37
NC_000003.10:g.170997180T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.908+47A>G MANE Select	ENSP00000414635.1:n.908+47A>G
ENST00000446859.5:c.908+47A>G	ENSP00000414635.1:n.908+47A>G
ENST00000522080.5:n.885+47A>G
ENST00000522329.1:n.157+47A>G
ENST00000522526.6:c.812+47A>G	ENSP00000429278.2:n.812+47A>G
ENST00000522596.6:n.890+47A>G
ENST00000522830.5:c.725+47A>G	ENSP00000429593.1:n.725+47A>G
ENST00000524327.5:n.708+47A>G
ENST00000528597.1:c.155+47A>G	ENSP00000436883.1:n.155+47A>G
ENST00000602774.1:n.341A>G
NM_001172779.1:c.908+47A>G	NP_001166250.1:n.908+47A>G
NM_001172780.1:c.908+47A>G	NP_001166251.1:n.908+47A>G
NM_153353.4:c.812+47A>G	NP_699184.2:n.812+47A>G
XM_005247133.2:c.725+47A>G	XP_005247190.1:n.725+47A>G
XM_006713508.2:c.854+47A>G	XP_006713571.1:n.854+47A>G
XM_011512442.1:c.905+47A>G	XP_011510744.1:n.905+47A>G
NM_001363888.1:c.725+47A>G	NP_001350817.1:n.725+47A>G
XM_006713508.4:c.854+47A>G	XP_006713571.1:n.854+47A>G
XM_011512442.2:c.905+47A>G	XP_011510744.1:n.905+47A>G
XM_017005746.1:c.722+47A>G	XP_016861235.1:n.722+47A>G
NM_001172779.2:c.908+47A>G MANE Select	NP_001166250.1:n.908+47A>G
NM_001172780.2:c.908+47A>G	NP_001166251.1:n.908+47A>G
NM_001363888.2:c.725+47A>G	NP_001350817.1:n.725+47A>G
NM_001370608.1:c.722+47A>G	NP_001357537.1:n.722+47A>G
NM_001370609.1:c.725+47A>G	NP_001357538.1:n.725+47A>G
NM_153353.5:c.812+47A>G	NP_699184.2:n.812+47A>G