Canonical Allele Identifier: CA436763684

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514607T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796819T>A , CM000665.2:g.169796819T>A	GRCh38
NC_000003.11:g.169514607T>A , CM000665.1:g.169514607T>A	GRCh37
NC_000003.10:g.170997301T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.834A>T MANE Select	ENSP00000414635.1:p.Ile278=
ENST00000446859.5:c.834A>T	ENSP00000414635.1:p.Ile278=
ENST00000522080.5:n.811A>T
ENST00000522329.1:n.83A>T
ENST00000522526.6:c.738A>T	ENSP00000429278.2:p.Ile246=
ENST00000522596.6:n.816A>T
ENST00000522830.5:c.651A>T	ENSP00000429593.1:p.Ile217=
ENST00000524054.5:n.682A>T
ENST00000524327.5:n.634A>T
ENST00000528597.1:c.81A>T	ENSP00000436883.1:p.Ile27=
ENST00000602774.1:n.220A>T
NM_001172779.1:c.834A>T	NP_001166250.1:p.Ile278=
NM_001172780.1:c.834A>T	NP_001166251.1:p.Ile278=
NM_153353.4:c.738A>T	NP_699184.2:p.Ile246=
XM_005247133.2:c.651A>T	XP_005247190.1:p.Ile217=
XM_006713508.2:c.780A>T	XP_006713571.1:p.Ile260=
XM_011512442.1:c.831A>T	XP_011510744.1:p.Ile277=
NM_001363888.1:c.651A>T	NP_001350817.1:p.Ile217=
XM_006713508.4:c.780A>T	XP_006713571.1:p.Ile260=
XM_011512442.2:c.831A>T	XP_011510744.1:p.Ile277=
XM_017005746.1:c.648A>T	XP_016861235.1:p.Ile216=
NM_001172779.2:c.834A>T MANE Select	NP_001166250.1:p.Ile278=
NM_001172780.2:c.834A>T	NP_001166251.1:p.Ile278=
NM_001363888.2:c.651A>T	NP_001350817.1:p.Ile217=
NM_001370608.1:c.648A>T	NP_001357537.1:p.Ile216=
NM_001370609.1:c.651A>T	NP_001357538.1:p.Ile217=
NM_153353.5:c.738A>T	NP_699184.2:p.Ile246=