Canonical Allele Identifier: CA436763715

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514673G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796885G>C , CM000665.2:g.169796885G>C	GRCh38
NC_000003.11:g.169514673G>C , CM000665.1:g.169514673G>C	GRCh37
NC_000003.10:g.170997367G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.768C>G MANE Select	ENSP00000414635.1:p.Val256=
ENST00000446859.5:c.768C>G	ENSP00000414635.1:p.Val256=
ENST00000522080.5:n.745C>G
ENST00000522329.1:n.17C>G
ENST00000522526.6:c.672C>G	ENSP00000429278.2:p.Val224=
ENST00000522596.6:n.750C>G
ENST00000522830.5:c.585C>G	ENSP00000429593.1:p.Val195=
ENST00000524054.5:n.616C>G
ENST00000524327.5:n.568C>G
ENST00000528597.1:c.15C>G	ENSP00000436883.1:p.Val5=
ENST00000602774.1:n.154C>G
NM_001172779.1:c.768C>G	NP_001166250.1:p.Val256=
NM_001172780.1:c.768C>G	NP_001166251.1:p.Val256=
NM_153353.4:c.672C>G	NP_699184.2:p.Val224=
XM_005247133.2:c.585C>G	XP_005247190.1:p.Val195=
XM_006713508.2:c.714C>G	XP_006713571.1:p.Val238=
XM_011512442.1:c.765C>G	XP_011510744.1:p.Val255=
NM_001363888.1:c.585C>G	NP_001350817.1:p.Val195=
XM_006713508.4:c.714C>G	XP_006713571.1:p.Val238=
XM_011512442.2:c.765C>G	XP_011510744.1:p.Val255=
XM_017005746.1:c.582C>G	XP_016861235.1:p.Val194=
NM_001172779.2:c.768C>G MANE Select	NP_001166250.1:p.Val256=
NM_001172780.2:c.768C>G	NP_001166251.1:p.Val256=
NM_001363888.2:c.585C>G	NP_001350817.1:p.Val195=
NM_001370608.1:c.582C>G	NP_001357537.1:p.Val194=
NM_001370609.1:c.585C>G	NP_001357538.1:p.Val195=
NM_153353.5:c.672C>G	NP_699184.2:p.Val224=