Canonical Allele Identifier: CA355076535

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514678T>A (hg19) ; chr3:g.169796890T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796890T>A , CM000665.2:g.169796890T>A	GRCh38
NC_000003.11:g.169514678T>A , CM000665.1:g.169514678T>A	GRCh37
NC_000003.10:g.170997372T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.763A>T MANE Select	ENSP00000414635.1:p.Thr255Ser
ENST00000446859.5:c.763A>T	ENSP00000414635.1:p.Thr255Ser
ENST00000522080.5:n.740A>T
ENST00000522329.1:n.12A>T
ENST00000522526.6:c.667A>T	ENSP00000429278.2:p.Thr223Ser
ENST00000522596.6:n.745A>T
ENST00000522830.5:c.580A>T	ENSP00000429593.1:p.Thr194Ser
ENST00000524054.5:n.611A>T
ENST00000524327.5:n.563A>T
ENST00000528597.1:c.10A>T	ENSP00000436883.1:p.Thr4Ser
ENST00000602774.1:n.149A>T
NM_001172779.1:c.763A>T	NP_001166250.1:p.Thr255Ser
NM_001172780.1:c.763A>T	NP_001166251.1:p.Thr255Ser
NM_153353.4:c.667A>T	NP_699184.2:p.Thr223Ser
XM_005247133.2:c.580A>T	XP_005247190.1:p.Thr194Ser
XM_006713508.2:c.709A>T	XP_006713571.1:p.Thr237Ser
XM_011512442.1:c.760A>T	XP_011510744.1:p.Thr254Ser
NM_001363888.1:c.580A>T	NP_001350817.1:p.Thr194Ser
XM_006713508.4:c.709A>T	XP_006713571.1:p.Thr237Ser
XM_011512442.2:c.760A>T	XP_011510744.1:p.Thr254Ser
XM_017005746.1:c.577A>T	XP_016861235.1:p.Thr193Ser
NM_001172779.2:c.763A>T MANE Select	NP_001166250.1:p.Thr255Ser
NM_001172780.2:c.763A>T	NP_001166251.1:p.Thr255Ser
NM_001363888.2:c.580A>T	NP_001350817.1:p.Thr194Ser
NM_001370608.1:c.577A>T	NP_001357537.1:p.Thr193Ser
NM_001370609.1:c.580A>T	NP_001357538.1:p.Thr194Ser
NM_153353.5:c.667A>T	NP_699184.2:p.Thr223Ser