Canonical Allele Identifier: CA355077177

Gene: LRRC34

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169800665A>T , CM000665.2:g.169800665A>T	GRCh38
NC_000003.11:g.169518453A>T , CM000665.1:g.169518453A>T	GRCh37
NC_000003.10:g.171001147A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.747T>A MANE Select	ENSP00000414635.1:p.Ser249Arg
ENST00000446859.5:c.747T>A	ENSP00000414635.1:p.Ser249Arg
ENST00000522080.5:n.724T>A
ENST00000522526.6:c.657+3388T>A	ENSP00000429278.2:n.657+3388T>A
ENST00000522596.6:n.729T>A
ENST00000522830.5:c.564T>A	ENSP00000429593.1:p.Ser188Arg
ENST00000524054.5:n.595T>A
ENST00000524327.5:n.547T>A
NM_001172779.1:c.747T>A	NP_001166250.1:p.Ser249Arg
NM_001172780.1:c.747T>A	NP_001166251.1:p.Ser249Arg
NM_153353.4:c.657+3388T>A	NP_699184.2:n.657+3388T>A
XM_005247133.2:c.564T>A	XP_005247190.1:p.Ser188Arg
XM_006713508.2:c.693T>A	XP_006713571.1:p.Ser231Arg
XM_011512442.1:c.744T>A	XP_011510744.1:p.Ser248Arg
NM_001363888.1:c.564T>A	NP_001350817.1:p.Ser188Arg
XM_006713508.4:c.693T>A	XP_006713571.1:p.Ser231Arg
XM_011512442.2:c.744T>A	XP_011510744.1:p.Ser248Arg
XM_017005746.1:c.561T>A	XP_016861235.1:p.Ser187Arg
NM_001172779.2:c.747T>A MANE Select	NP_001166250.1:p.Ser249Arg
NM_001172780.2:c.747T>A	NP_001166251.1:p.Ser249Arg
NM_001363888.2:c.564T>A	NP_001350817.1:p.Ser188Arg
NM_001370608.1:c.561T>A	NP_001357537.1:p.Ser187Arg
NM_001370609.1:c.564T>A	NP_001357538.1:p.Ser188Arg
NM_153353.5:c.657+3388T>A	NP_699184.2:n.657+3388T>A