Canonical Allele Identifier: CA355076282

Gene: LRRC34

Linked Data

• gnomAD v4: 3-169796857-G-A
• MyVariant Identifiers: chr3:g.169514645G>A (hg19) ; chr3:g.169796857G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796857G>A , CM000665.2:g.169796857G>A	GRCh38
NC_000003.11:g.169514645G>A , CM000665.1:g.169514645G>A	GRCh37
NC_000003.10:g.170997339G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.796C>T MANE Select	ENSP00000414635.1:p.His266Tyr
ENST00000446859.5:c.796C>T	ENSP00000414635.1:p.His266Tyr
ENST00000522080.5:n.773C>T
ENST00000522329.1:n.45C>T
ENST00000522526.6:c.700C>T	ENSP00000429278.2:p.His234Tyr
ENST00000522596.6:n.778C>T
ENST00000522830.5:c.613C>T	ENSP00000429593.1:p.His205Tyr
ENST00000524054.5:n.644C>T
ENST00000524327.5:n.596C>T
ENST00000528597.1:c.43C>T	ENSP00000436883.1:p.His15Tyr
ENST00000602774.1:n.182C>T
NM_001172779.1:c.796C>T	NP_001166250.1:p.His266Tyr
NM_001172780.1:c.796C>T	NP_001166251.1:p.His266Tyr
NM_153353.4:c.700C>T	NP_699184.2:p.His234Tyr
XM_005247133.2:c.613C>T	XP_005247190.1:p.His205Tyr
XM_006713508.2:c.742C>T	XP_006713571.1:p.His248Tyr
XM_011512442.1:c.793C>T	XP_011510744.1:p.His265Tyr
NM_001363888.1:c.613C>T	NP_001350817.1:p.His205Tyr
XM_006713508.4:c.742C>T	XP_006713571.1:p.His248Tyr
XM_011512442.2:c.793C>T	XP_011510744.1:p.His265Tyr
XM_017005746.1:c.610C>T	XP_016861235.1:p.His204Tyr
NM_001172779.2:c.796C>T MANE Select	NP_001166250.1:p.His266Tyr
NM_001172780.2:c.796C>T	NP_001166251.1:p.His266Tyr
NM_001363888.2:c.613C>T	NP_001350817.1:p.His205Tyr
NM_001370608.1:c.610C>T	NP_001357537.1:p.His204Tyr
NM_001370609.1:c.613C>T	NP_001357538.1:p.His205Tyr
NM_153353.5:c.700C>T	NP_699184.2:p.His234Tyr