Canonical Allele Identifier: CA355076501

Gene: LRRC34

Linked Data

• dbSNP Id: rs1560596457
• MyVariant Identifiers: chr3:g.169514671T>G (hg19) ; chr3:g.169796883T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796883T>G , CM000665.2:g.169796883T>G	GRCh38
NC_000003.11:g.169514671T>G , CM000665.1:g.169514671T>G	GRCh37
NC_000003.10:g.170997365T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.770A>C MANE Select	ENSP00000414635.1:p.His257Pro
ENST00000446859.5:c.770A>C	ENSP00000414635.1:p.His257Pro
ENST00000522080.5:n.747A>C
ENST00000522329.1:n.19A>C
ENST00000522526.6:c.674A>C	ENSP00000429278.2:p.His225Pro
ENST00000522596.6:n.752A>C
ENST00000522830.5:c.587A>C	ENSP00000429593.1:p.His196Pro
ENST00000524054.5:n.618A>C
ENST00000524327.5:n.570A>C
ENST00000528597.1:c.17A>C	ENSP00000436883.1:p.His6Pro
ENST00000602774.1:n.156A>C
NM_001172779.1:c.770A>C	NP_001166250.1:p.His257Pro
NM_001172780.1:c.770A>C	NP_001166251.1:p.His257Pro
NM_153353.4:c.674A>C	NP_699184.2:p.His225Pro
XM_005247133.2:c.587A>C	XP_005247190.1:p.His196Pro
XM_006713508.2:c.716A>C	XP_006713571.1:p.His239Pro
XM_011512442.1:c.767A>C	XP_011510744.1:p.His256Pro
NM_001363888.1:c.587A>C	NP_001350817.1:p.His196Pro
XM_006713508.4:c.716A>C	XP_006713571.1:p.His239Pro
XM_011512442.2:c.767A>C	XP_011510744.1:p.His256Pro
XM_017005746.1:c.584A>C	XP_016861235.1:p.His195Pro
NM_001172779.2:c.770A>C MANE Select	NP_001166250.1:p.His257Pro
NM_001172780.2:c.770A>C	NP_001166251.1:p.His257Pro
NM_001363888.2:c.587A>C	NP_001350817.1:p.His196Pro
NM_001370608.1:c.584A>C	NP_001357537.1:p.His195Pro
NM_001370609.1:c.587A>C	NP_001357538.1:p.His196Pro
NM_153353.5:c.674A>C	NP_699184.2:p.His225Pro