Canonical Allele Identifier: CA495962216

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409287C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375384C>T , CM000678.2:g.67375384C>T	GRCh38
NC_000016.9:g.67409287C>T , CM000678.1:g.67409287C>T	GRCh37
NC_000016.8:g.65966788C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1632C>T MANE Select	ENSP00000329943.6:p.Gly544=
ENST00000329956.10:c.1632C>T	ENSP00000329943.6:p.Gly544=
ENST00000435835.3:c.1132-3205C>T	ENSP00000411122.3:n.1132-3205C>T
ENST00000563189.5:c.1269C>T	ENSP00000455103.1:p.Gly423=
ENST00000565019.6:c.1141C>T
ENST00000567723.5:c.*958C>T	ENSP00000455799.1:n.*958C>T
ENST00000567823.5:c.*127C>T	ENSP00000456164.1:n.*127C>T
ENST00000568010.5:c.*372C>T	ENSP00000455018.1:n.*372C>T
NM_001161575.1:c.1269C>T	NP_001155047.1:p.Gly423=
NM_018296.5:c.1632C>T	NP_060766.5:p.Gly544=
XM_005256025.2:c.1632C>T	XP_005256082.1:p.Gly544=
XM_005256026.2:c.1191C>T	XP_005256083.1:p.Gly397=
XM_005256027.2:c.1632C>T	XP_005256084.1:p.Gly544=
XM_005256028.1:c.1128C>T	XP_005256085.1:p.Gly376=
XM_011523199.1:c.1632C>T	XP_011521501.1:p.Gly544=
XM_011523200.1:c.1632C>T	XP_011521502.1:p.Gly544=
XM_011523201.1:c.1128C>T	XP_011521503.1:p.Gly376=
XM_011523202.1:c.1125C>T	XP_011521504.1:p.Gly375=
XM_011523203.1:c.1014C>T	XP_011521505.1:p.Gly338=
XM_011523204.1:c.906C>T	XP_011521506.1:p.Gly302=
XM_011523205.1:c.906C>T	XP_011521507.1:p.Gly302=
XR_243416.2:n.1651C>T
XR_429723.1:n.1640C>T
XM_011523202.2:c.1125C>T	XP_011521504.1:p.Gly375=
XM_017023400.2:c.1632C>T	XP_016878889.1:p.Gly544=
XM_017023401.1:c.881C>T	XP_016878890.1:p.Ala294Val
XM_017023402.1:c.704C>T	XP_016878891.1:p.Ala235Val
XM_024450338.1:c.906C>T	XP_024306106.1:p.Gly302=
NM_018296.6:c.1632C>T MANE Select	NP_060766.5:p.Gly544=
NM_001161575.2:c.1269C>T	NP_001155047.1:p.Gly423=