Canonical Allele Identifier: CA355076400

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514658C>T (hg19) ; chr3:g.169796870C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796870C>T , CM000665.2:g.169796870C>T	GRCh38
NC_000003.11:g.169514658C>T , CM000665.1:g.169514658C>T	GRCh37
NC_000003.10:g.170997352C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.783G>A MANE Select	ENSP00000414635.1:p.Met261Ile
ENST00000446859.5:c.783G>A	ENSP00000414635.1:p.Met261Ile
ENST00000522080.5:n.760G>A
ENST00000522329.1:n.32G>A
ENST00000522526.6:c.687G>A	ENSP00000429278.2:p.Met229Ile
ENST00000522596.6:n.765G>A
ENST00000522830.5:c.600G>A	ENSP00000429593.1:p.Met200Ile
ENST00000524054.5:n.631G>A
ENST00000524327.5:n.583G>A
ENST00000528597.1:c.30G>A	ENSP00000436883.1:p.Met10Ile
ENST00000602774.1:n.169G>A
NM_001172779.1:c.783G>A	NP_001166250.1:p.Met261Ile
NM_001172780.1:c.783G>A	NP_001166251.1:p.Met261Ile
NM_153353.4:c.687G>A	NP_699184.2:p.Met229Ile
XM_005247133.2:c.600G>A	XP_005247190.1:p.Met200Ile
XM_006713508.2:c.729G>A	XP_006713571.1:p.Met243Ile
XM_011512442.1:c.780G>A	XP_011510744.1:p.Met260Ile
NM_001363888.1:c.600G>A	NP_001350817.1:p.Met200Ile
XM_006713508.4:c.729G>A	XP_006713571.1:p.Met243Ile
XM_011512442.2:c.780G>A	XP_011510744.1:p.Met260Ile
XM_017005746.1:c.597G>A	XP_016861235.1:p.Met199Ile
NM_001172779.2:c.783G>A MANE Select	NP_001166250.1:p.Met261Ile
NM_001172780.2:c.783G>A	NP_001166251.1:p.Met261Ile
NM_001363888.2:c.600G>A	NP_001350817.1:p.Met200Ile
NM_001370608.1:c.597G>A	NP_001357537.1:p.Met199Ile
NM_001370609.1:c.600G>A	NP_001357538.1:p.Met200Ile
NM_153353.5:c.687G>A	NP_699184.2:p.Met229Ile