Canonical Allele Identifier: CA396268242

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409218A>C (hg19) ; chr16:g.67375315A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375315A>C , CM000678.2:g.67375315A>C	GRCh38
NC_000016.9:g.67409218A>C , CM000678.1:g.67409218A>C	GRCh37
NC_000016.8:g.65966719A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1563A>C MANE Select	ENSP00000329943.6:p.Arg521Ser
ENST00000329956.10:c.1563A>C	ENSP00000329943.6:p.Arg521Ser
ENST00000435835.3:c.1132-3274A>C	ENSP00000411122.3:n.1132-3274A>C
ENST00000563189.5:c.1200A>C	ENSP00000455103.1:p.Arg400Ser
ENST00000565019.6:c.1072A>C
ENST00000567723.5:c.*889A>C	ENSP00000455799.1:n.*889A>C
ENST00000567823.5:c.*58A>C	ENSP00000456164.1:n.*58A>C
ENST00000568010.5:c.*303A>C	ENSP00000455018.1:n.*303A>C
NM_001161575.1:c.1200A>C	NP_001155047.1:p.Arg400Ser
NM_018296.5:c.1563A>C	NP_060766.5:p.Arg521Ser
XM_005256025.2:c.1563A>C	XP_005256082.1:p.Arg521Ser
XM_005256026.2:c.1122A>C	XP_005256083.1:p.Arg374Ser
XM_005256027.2:c.1563A>C	XP_005256084.1:p.Arg521Ser
XM_005256028.1:c.1059A>C	XP_005256085.1:p.Arg353Ser
XM_011523199.1:c.1563A>C	XP_011521501.1:p.Arg521Ser
XM_011523200.1:c.1563A>C	XP_011521502.1:p.Arg521Ser
XM_011523201.1:c.1059A>C	XP_011521503.1:p.Arg353Ser
XM_011523202.1:c.1056A>C	XP_011521504.1:p.Arg352Ser
XM_011523203.1:c.945A>C	XP_011521505.1:p.Arg315Ser
XM_011523204.1:c.837A>C	XP_011521506.1:p.Arg279Ser
XM_011523205.1:c.837A>C	XP_011521507.1:p.Arg279Ser
XR_243416.2:n.1582A>C
XR_429723.1:n.1571A>C
XM_011523202.2:c.1056A>C	XP_011521504.1:p.Arg352Ser
XM_017023400.2:c.1563A>C	XP_016878889.1:p.Arg521Ser
XM_017023401.1:c.812A>C	XP_016878890.1:p.Glu271Ala
XM_017023402.1:c.635A>C	XP_016878891.1:p.Glu212Ala
XM_024450338.1:c.837A>C	XP_024306106.1:p.Arg279Ser
NM_018296.6:c.1563A>C MANE Select	NP_060766.5:p.Arg521Ser
NM_001161575.2:c.1200A>C	NP_001155047.1:p.Arg400Ser