Canonical Allele Identifier: CA1419615122

Gene: LRRC34

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169810661C>G , CM000665.2:g.169810661C>G	GRCh38
NC_000003.11:g.169528449C>G , CM000665.1:g.169528449C>G	GRCh37
NC_000003.10:g.171011143C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446859.7:c.139+1749G>C MANE Select	ENSP00000414635.1:n.139+1749G>C
ENST00000446859.5:c.139+1749G>C	ENSP00000414635.1:n.139+1749G>C
ENST00000522080.5:n.116+1749G>C
ENST00000522526.6:c.139+1749G>C	ENSP00000429278.2:n.139+1749G>C
ENST00000522596.6:n.121+1909G>C
ENST00000522830.5:c.-45+1909G>C	ENSP00000429593.1:n.-45+1909G>C
ENST00000524054.5:n.105+1749G>C
NM_001172779.1:c.139+1749G>C	NP_001166250.1:n.139+1749G>C
NM_001172780.1:c.139+1749G>C	NP_001166251.1:n.139+1749G>C
NM_153353.4:c.139+1749G>C	NP_699184.2:n.139+1749G>C
XM_005247133.2:c.-45+1909G>C	XP_005247190.1:n.-45+1909G>C
XM_006713508.2:c.139+1749G>C	XP_006713571.1:n.139+1749G>C
XM_011512442.1:c.139+1749G>C	XP_011510744.1:n.139+1749G>C
NM_001363888.1:c.-45+1909G>C	NP_001350817.1:n.-45+1909G>C
XM_006713508.4:c.139+1749G>C	XP_006713571.1:n.139+1749G>C
XM_011512442.2:c.139+1749G>C	XP_011510744.1:n.139+1749G>C
XM_017005746.1:c.-45+1909G>C	XP_016861235.1:n.-45+1909G>C
NM_001172779.2:c.139+1749G>C MANE Select	NP_001166250.1:n.139+1749G>C
NM_001172780.2:c.139+1749G>C	NP_001166251.1:n.139+1749G>C
NM_001363888.2:c.-45+1909G>C	NP_001350817.1:n.-45+1909G>C
NM_001370608.1:c.-45+1909G>C	NP_001357537.1:n.-45+1909G>C
NM_001370609.1:c.-45+1909G>C	NP_001357538.1:n.-45+1909G>C
NM_153353.5:c.139+1749G>C	NP_699184.2:n.139+1749G>C