Canonical Allele Identifier: CA396267886

Gene: LRRC36

Linked Data

• gnomAD v4: 16-67375269-G-C
• MyVariant Identifiers: chr16:g.67409172G>C (hg19) ; chr16:g.67375269G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375269G>C , CM000678.2:g.67375269G>C	GRCh38
NC_000016.9:g.67409172G>C , CM000678.1:g.67409172G>C	GRCh37
NC_000016.8:g.65966673G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1517G>C MANE Select	ENSP00000329943.6:p.Ser506Thr
ENST00000329956.10:c.1517G>C	ENSP00000329943.6:p.Ser506Thr
ENST00000435835.3:c.1132-3320G>C	ENSP00000411122.3:n.1132-3320G>C
ENST00000563189.5:c.1154G>C	ENSP00000455103.1:p.Ser385Thr
ENST00000565019.6:c.1072-46G>C
ENST00000567723.5:c.*843G>C	ENSP00000455799.1:n.*843G>C
ENST00000567823.5:c.*12G>C	ENSP00000456164.1:n.*12G>C
ENST00000568010.5:c.*257G>C	ENSP00000455018.1:n.*257G>C
NM_001161575.1:c.1154G>C	NP_001155047.1:p.Ser385Thr
NM_018296.5:c.1517G>C	NP_060766.5:p.Ser506Thr
XM_005256025.2:c.1517G>C	XP_005256082.1:p.Ser506Thr
XM_005256026.2:c.1076G>C	XP_005256083.1:p.Ser359Thr
XM_005256027.2:c.1517G>C	XP_005256084.1:p.Ser506Thr
XM_005256028.1:c.1013G>C	XP_005256085.1:p.Ser338Thr
XM_011523199.1:c.1517G>C	XP_011521501.1:p.Ser506Thr
XM_011523200.1:c.1517G>C	XP_011521502.1:p.Ser506Thr
XM_011523201.1:c.1013G>C	XP_011521503.1:p.Ser338Thr
XM_011523202.1:c.1010G>C	XP_011521504.1:p.Ser337Thr
XM_011523203.1:c.899G>C	XP_011521505.1:p.Ser300Thr
XM_011523204.1:c.791G>C	XP_011521506.1:p.Ser264Thr
XM_011523205.1:c.791G>C	XP_011521507.1:p.Ser264Thr
XR_243416.2:n.1536G>C
XR_429723.1:n.1525G>C
XM_011523202.2:c.1010G>C	XP_011521504.1:p.Ser337Thr
XM_017023400.2:c.1517G>C	XP_016878889.1:p.Ser506Thr
XM_017023401.1:c.766G>C	XP_016878890.1:p.Val256Leu
XM_017023402.1:c.589G>C	XP_016878891.1:p.Val197Leu
XM_024450338.1:c.791G>C	XP_024306106.1:p.Ser264Thr
NM_018296.6:c.1517G>C MANE Select	NP_060766.5:p.Ser506Thr
NM_001161575.2:c.1154G>C	NP_001155047.1:p.Ser385Thr