Canonical Allele Identifier: CA495962223

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409290C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375387C>G , CM000678.2:g.67375387C>G	GRCh38
NC_000016.9:g.67409290C>G , CM000678.1:g.67409290C>G	GRCh37
NC_000016.8:g.65966791C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1635C>G MANE Select	ENSP00000329943.6:p.Ser545=
ENST00000329956.10:c.1635C>G	ENSP00000329943.6:p.Ser545=
ENST00000435835.3:c.1132-3202C>G	ENSP00000411122.3:n.1132-3202C>G
ENST00000563189.5:c.1272C>G	ENSP00000455103.1:p.Ser424=
ENST00000565019.6:c.1144C>G
ENST00000567723.5:c.*961C>G	ENSP00000455799.1:n.*961C>G
ENST00000567823.5:c.*130C>G	ENSP00000456164.1:n.*130C>G
ENST00000568010.5:c.*375C>G	ENSP00000455018.1:n.*375C>G
NM_001161575.1:c.1272C>G	NP_001155047.1:p.Ser424=
NM_018296.5:c.1635C>G	NP_060766.5:p.Ser545=
XM_005256025.2:c.1635C>G	XP_005256082.1:p.Ser545=
XM_005256026.2:c.1194C>G	XP_005256083.1:p.Ser398=
XM_005256027.2:c.1635C>G	XP_005256084.1:p.Ser545=
XM_005256028.1:c.1131C>G	XP_005256085.1:p.Ser377=
XM_011523199.1:c.1635C>G	XP_011521501.1:p.Ser545=
XM_011523200.1:c.1635C>G	XP_011521502.1:p.Ser545=
XM_011523201.1:c.1131C>G	XP_011521503.1:p.Ser377=
XM_011523202.1:c.1128C>G	XP_011521504.1:p.Ser376=
XM_011523203.1:c.1017C>G	XP_011521505.1:p.Ser339=
XM_011523204.1:c.909C>G	XP_011521506.1:p.Ser303=
XM_011523205.1:c.909C>G	XP_011521507.1:p.Ser303=
XR_243416.2:n.1654C>G
XR_429723.1:n.1643C>G
XM_011523202.2:c.1128C>G	XP_011521504.1:p.Ser376=
XM_017023400.2:c.1635C>G	XP_016878889.1:p.Ser545=
XM_017023401.1:c.884C>G	XP_016878890.1:p.Pro295Arg
XM_017023402.1:c.707C>G	XP_016878891.1:p.Pro236Arg
XM_024450338.1:c.909C>G	XP_024306106.1:p.Ser303=
NM_018296.6:c.1635C>G MANE Select	NP_060766.5:p.Ser545=
NM_001161575.2:c.1272C>G	NP_001155047.1:p.Ser424=