Canonical Allele Identifier: CA355076489

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514669C>A (hg19) ; chr3:g.169796881C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796881C>A , CM000665.2:g.169796881C>A	GRCh38
NC_000003.11:g.169514669C>A , CM000665.1:g.169514669C>A	GRCh37
NC_000003.10:g.170997363C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.772G>T MANE Select	ENSP00000414635.1:p.Val258Leu
ENST00000446859.5:c.772G>T	ENSP00000414635.1:p.Val258Leu
ENST00000522080.5:n.749G>T
ENST00000522329.1:n.21G>T
ENST00000522526.6:c.676G>T	ENSP00000429278.2:p.Val226Leu
ENST00000522596.6:n.754G>T
ENST00000522830.5:c.589G>T	ENSP00000429593.1:p.Val197Leu
ENST00000524054.5:n.620G>T
ENST00000524327.5:n.572G>T
ENST00000528597.1:c.19G>T	ENSP00000436883.1:p.Val7Leu
ENST00000602774.1:n.158G>T
NM_001172779.1:c.772G>T	NP_001166250.1:p.Val258Leu
NM_001172780.1:c.772G>T	NP_001166251.1:p.Val258Leu
NM_153353.4:c.676G>T	NP_699184.2:p.Val226Leu
XM_005247133.2:c.589G>T	XP_005247190.1:p.Val197Leu
XM_006713508.2:c.718G>T	XP_006713571.1:p.Val240Leu
XM_011512442.1:c.769G>T	XP_011510744.1:p.Val257Leu
NM_001363888.1:c.589G>T	NP_001350817.1:p.Val197Leu
XM_006713508.4:c.718G>T	XP_006713571.1:p.Val240Leu
XM_011512442.2:c.769G>T	XP_011510744.1:p.Val257Leu
XM_017005746.1:c.586G>T	XP_016861235.1:p.Val196Leu
NM_001172779.2:c.772G>T MANE Select	NP_001166250.1:p.Val258Leu
NM_001172780.2:c.772G>T	NP_001166251.1:p.Val258Leu
NM_001363888.2:c.589G>T	NP_001350817.1:p.Val197Leu
NM_001370608.1:c.586G>T	NP_001357537.1:p.Val196Leu
NM_001370609.1:c.589G>T	NP_001357538.1:p.Val197Leu
NM_153353.5:c.676G>T	NP_699184.2:p.Val226Leu