Canonical Allele Identifier: CA355076428

Gene: LRRC34

Linked Data

• dbSNP Id: rs1280781281
• gnomAD v3: 3-169796872-T-C
• gnomAD v4: 3-169796872-T-C
• MyVariant Identifiers: chr3:g.169514660T>C (hg19) ; chr3:g.169796872T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796872T>C , CM000665.2:g.169796872T>C	GRCh38
NC_000003.11:g.169514660T>C , CM000665.1:g.169514660T>C	GRCh37
NC_000003.10:g.170997354T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.781A>G MANE Select	ENSP00000414635.1:p.Met261Val
ENST00000446859.5:c.781A>G	ENSP00000414635.1:p.Met261Val
ENST00000522080.5:n.758A>G
ENST00000522329.1:n.30A>G
ENST00000522526.6:c.685A>G	ENSP00000429278.2:p.Met229Val
ENST00000522596.6:n.763A>G
ENST00000522830.5:c.598A>G	ENSP00000429593.1:p.Met200Val
ENST00000524054.5:n.629A>G
ENST00000524327.5:n.581A>G
ENST00000528597.1:c.28A>G	ENSP00000436883.1:p.Met10Val
ENST00000602774.1:n.167A>G
NM_001172779.1:c.781A>G	NP_001166250.1:p.Met261Val
NM_001172780.1:c.781A>G	NP_001166251.1:p.Met261Val
NM_153353.4:c.685A>G	NP_699184.2:p.Met229Val
XM_005247133.2:c.598A>G	XP_005247190.1:p.Met200Val
XM_006713508.2:c.727A>G	XP_006713571.1:p.Met243Val
XM_011512442.1:c.778A>G	XP_011510744.1:p.Met260Val
NM_001363888.1:c.598A>G	NP_001350817.1:p.Met200Val
XM_006713508.4:c.727A>G	XP_006713571.1:p.Met243Val
XM_011512442.2:c.778A>G	XP_011510744.1:p.Met260Val
XM_017005746.1:c.595A>G	XP_016861235.1:p.Met199Val
NM_001172779.2:c.781A>G MANE Select	NP_001166250.1:p.Met261Val
NM_001172780.2:c.781A>G	NP_001166251.1:p.Met261Val
NM_001363888.2:c.598A>G	NP_001350817.1:p.Met200Val
NM_001370608.1:c.595A>G	NP_001357537.1:p.Met199Val
NM_001370609.1:c.598A>G	NP_001357538.1:p.Met200Val
NM_153353.5:c.685A>G	NP_699184.2:p.Met229Val