Canonical Allele Identifier: CA355076493

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514670A>C (hg19) ; chr3:g.169796882A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796882A>C , CM000665.2:g.169796882A>C	GRCh38
NC_000003.11:g.169514670A>C , CM000665.1:g.169514670A>C	GRCh37
NC_000003.10:g.170997364A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.771T>G MANE Select	ENSP00000414635.1:p.His257Gln
ENST00000446859.5:c.771T>G	ENSP00000414635.1:p.His257Gln
ENST00000522080.5:n.748T>G
ENST00000522329.1:n.20T>G
ENST00000522526.6:c.675T>G	ENSP00000429278.2:p.His225Gln
ENST00000522596.6:n.753T>G
ENST00000522830.5:c.588T>G	ENSP00000429593.1:p.His196Gln
ENST00000524054.5:n.619T>G
ENST00000524327.5:n.571T>G
ENST00000528597.1:c.18T>G	ENSP00000436883.1:p.His6Gln
ENST00000602774.1:n.157T>G
NM_001172779.1:c.771T>G	NP_001166250.1:p.His257Gln
NM_001172780.1:c.771T>G	NP_001166251.1:p.His257Gln
NM_153353.4:c.675T>G	NP_699184.2:p.His225Gln
XM_005247133.2:c.588T>G	XP_005247190.1:p.His196Gln
XM_006713508.2:c.717T>G	XP_006713571.1:p.His239Gln
XM_011512442.1:c.768T>G	XP_011510744.1:p.His256Gln
NM_001363888.1:c.588T>G	NP_001350817.1:p.His196Gln
XM_006713508.4:c.717T>G	XP_006713571.1:p.His239Gln
XM_011512442.2:c.768T>G	XP_011510744.1:p.His256Gln
XM_017005746.1:c.585T>G	XP_016861235.1:p.His195Gln
NM_001172779.2:c.771T>G MANE Select	NP_001166250.1:p.His257Gln
NM_001172780.2:c.771T>G	NP_001166251.1:p.His257Gln
NM_001363888.2:c.588T>G	NP_001350817.1:p.His196Gln
NM_001370608.1:c.585T>G	NP_001357537.1:p.His195Gln
NM_001370609.1:c.588T>G	NP_001357538.1:p.His196Gln
NM_153353.5:c.675T>G	NP_699184.2:p.His225Gln