Canonical Allele Identifier: CA355075732

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514598A>T (hg19) ; chr3:g.169796810A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796810A>T , CM000665.2:g.169796810A>T	GRCh38
NC_000003.11:g.169514598A>T , CM000665.1:g.169514598A>T	GRCh37
NC_000003.10:g.170997292A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.843T>A MANE Select	ENSP00000414635.1:p.Ser281Arg
ENST00000446859.5:c.843T>A	ENSP00000414635.1:p.Ser281Arg
ENST00000522080.5:n.820T>A
ENST00000522329.1:n.92T>A
ENST00000522526.6:c.747T>A	ENSP00000429278.2:p.Ser249Arg
ENST00000522596.6:n.825T>A
ENST00000522830.5:c.660T>A	ENSP00000429593.1:p.Ser220Arg
ENST00000524054.5:n.691T>A
ENST00000524327.5:n.643T>A
ENST00000528597.1:c.90T>A	ENSP00000436883.1:p.Ser30Arg
ENST00000602774.1:n.229T>A
NM_001172779.1:c.843T>A	NP_001166250.1:p.Ser281Arg
NM_001172780.1:c.843T>A	NP_001166251.1:p.Ser281Arg
NM_153353.4:c.747T>A	NP_699184.2:p.Ser249Arg
XM_005247133.2:c.660T>A	XP_005247190.1:p.Ser220Arg
XM_006713508.2:c.789T>A	XP_006713571.1:p.Ser263Arg
XM_011512442.1:c.840T>A	XP_011510744.1:p.Ser280Arg
NM_001363888.1:c.660T>A	NP_001350817.1:p.Ser220Arg
XM_006713508.4:c.789T>A	XP_006713571.1:p.Ser263Arg
XM_011512442.2:c.840T>A	XP_011510744.1:p.Ser280Arg
XM_017005746.1:c.657T>A	XP_016861235.1:p.Ser219Arg
NM_001172779.2:c.843T>A MANE Select	NP_001166250.1:p.Ser281Arg
NM_001172780.2:c.843T>A	NP_001166251.1:p.Ser281Arg
NM_001363888.2:c.660T>A	NP_001350817.1:p.Ser220Arg
NM_001370608.1:c.657T>A	NP_001357537.1:p.Ser219Arg
NM_001370609.1:c.660T>A	NP_001357538.1:p.Ser220Arg
NM_153353.5:c.747T>A	NP_699184.2:p.Ser249Arg