Canonical Allele Identifier: CA87604433

Gene: LRRC34

Linked Data

• dbSNP Id: rs146384166
• gnomAD v4: 3-169796867-C-T
• MyVariant Identifiers: chr3:g.169514655C>T (hg19) ; chr3:g.169796867C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796867C>T , CM000665.2:g.169796867C>T	GRCh38
NC_000003.11:g.169514655C>T , CM000665.1:g.169514655C>T	GRCh37
NC_000003.10:g.170997349C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.786G>A MANE Select	ENSP00000414635.1:p.Leu262=
ENST00000446859.5:c.786G>A	ENSP00000414635.1:p.Leu262=
ENST00000522080.5:n.763G>A
ENST00000522329.1:n.35G>A
ENST00000522526.6:c.690G>A	ENSP00000429278.2:p.Leu230=
ENST00000522596.6:n.768G>A
ENST00000522830.5:c.603G>A	ENSP00000429593.1:p.Leu201=
ENST00000524054.5:n.634G>A
ENST00000524327.5:n.586G>A
ENST00000528597.1:c.33G>A	ENSP00000436883.1:p.Leu11=
ENST00000602774.1:n.172G>A
NM_001172779.1:c.786G>A	NP_001166250.1:p.Leu262=
NM_001172780.1:c.786G>A	NP_001166251.1:p.Leu262=
NM_153353.4:c.690G>A	NP_699184.2:p.Leu230=
XM_005247133.2:c.603G>A	XP_005247190.1:p.Leu201=
XM_006713508.2:c.732G>A	XP_006713571.1:p.Leu244=
XM_011512442.1:c.783G>A	XP_011510744.1:p.Leu261=
NM_001363888.1:c.603G>A	NP_001350817.1:p.Leu201=
XM_006713508.4:c.732G>A	XP_006713571.1:p.Leu244=
XM_011512442.2:c.783G>A	XP_011510744.1:p.Leu261=
XM_017005746.1:c.600G>A	XP_016861235.1:p.Leu200=
NM_001172779.2:c.786G>A MANE Select	NP_001166250.1:p.Leu262=
NM_001172780.2:c.786G>A	NP_001166251.1:p.Leu262=
NM_001363888.2:c.603G>A	NP_001350817.1:p.Leu201=
NM_001370608.1:c.600G>A	NP_001357537.1:p.Leu200=
NM_001370609.1:c.603G>A	NP_001357538.1:p.Leu201=
NM_153353.5:c.690G>A	NP_699184.2:p.Leu230=