Canonical Allele Identifier: CA355075372

Gene: LRRC34

Linked Data

• MyVariant Identifiers: chr3:g.169514560C>A (hg19) ; chr3:g.169796772C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169796772C>A , CM000665.2:g.169796772C>A	GRCh38
NC_000003.11:g.169514560C>A , CM000665.1:g.169514560C>A	GRCh37
NC_000003.10:g.170997254C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.881G>T MANE Select	ENSP00000414635.1:p.Ser294Ile
ENST00000446859.5:c.881G>T	ENSP00000414635.1:p.Ser294Ile
ENST00000522080.5:n.858G>T
ENST00000522329.1:n.130G>T
ENST00000522526.6:c.785G>T	ENSP00000429278.2:p.Ser262Ile
ENST00000522596.6:n.863G>T
ENST00000522830.5:c.698G>T	ENSP00000429593.1:p.Ser233Ile
ENST00000524054.5:n.729G>T
ENST00000524327.5:n.681G>T
ENST00000528597.1:c.128G>T	ENSP00000436883.1:p.Ser43Ile
ENST00000602774.1:n.267G>T
NM_001172779.1:c.881G>T	NP_001166250.1:p.Ser294Ile
NM_001172780.1:c.881G>T	NP_001166251.1:p.Ser294Ile
NM_153353.4:c.785G>T	NP_699184.2:p.Ser262Ile
XM_005247133.2:c.698G>T	XP_005247190.1:p.Ser233Ile
XM_006713508.2:c.827G>T	XP_006713571.1:p.Ser276Ile
XM_011512442.1:c.878G>T	XP_011510744.1:p.Ser293Ile
NM_001363888.1:c.698G>T	NP_001350817.1:p.Ser233Ile
XM_006713508.4:c.827G>T	XP_006713571.1:p.Ser276Ile
XM_011512442.2:c.878G>T	XP_011510744.1:p.Ser293Ile
XM_017005746.1:c.695G>T	XP_016861235.1:p.Ser232Ile
NM_001172779.2:c.881G>T MANE Select	NP_001166250.1:p.Ser294Ile
NM_001172780.2:c.881G>T	NP_001166251.1:p.Ser294Ile
NM_001363888.2:c.698G>T	NP_001350817.1:p.Ser233Ile
NM_001370608.1:c.695G>T	NP_001357537.1:p.Ser232Ile
NM_001370609.1:c.698G>T	NP_001357538.1:p.Ser233Ile
NM_153353.5:c.785G>T	NP_699184.2:p.Ser262Ile