Canonical Allele Identifier: CA396270186

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409286G>T (hg19) ; chr16:g.67375383G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375383G>T , CM000678.2:g.67375383G>T	GRCh38
NC_000016.9:g.67409286G>T , CM000678.1:g.67409286G>T	GRCh37
NC_000016.8:g.65966787G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1631G>T MANE Select	ENSP00000329943.6:p.Gly544Val
ENST00000329956.10:c.1631G>T	ENSP00000329943.6:p.Gly544Val
ENST00000435835.3:c.1132-3206G>T	ENSP00000411122.3:n.1132-3206G>T
ENST00000563189.5:c.1268G>T	ENSP00000455103.1:p.Gly423Val
ENST00000565019.6:c.1140G>T
ENST00000567723.5:c.*957G>T	ENSP00000455799.1:n.*957G>T
ENST00000567823.5:c.*126G>T	ENSP00000456164.1:n.*126G>T
ENST00000568010.5:c.*371G>T	ENSP00000455018.1:n.*371G>T
NM_001161575.1:c.1268G>T	NP_001155047.1:p.Gly423Val
NM_018296.5:c.1631G>T	NP_060766.5:p.Gly544Val
XM_005256025.2:c.1631G>T	XP_005256082.1:p.Gly544Val
XM_005256026.2:c.1190G>T	XP_005256083.1:p.Gly397Val
XM_005256027.2:c.1631G>T	XP_005256084.1:p.Gly544Val
XM_005256028.1:c.1127G>T	XP_005256085.1:p.Gly376Val
XM_011523199.1:c.1631G>T	XP_011521501.1:p.Gly544Val
XM_011523200.1:c.1631G>T	XP_011521502.1:p.Gly544Val
XM_011523201.1:c.1127G>T	XP_011521503.1:p.Gly376Val
XM_011523202.1:c.1124G>T	XP_011521504.1:p.Gly375Val
XM_011523203.1:c.1013G>T	XP_011521505.1:p.Gly338Val
XM_011523204.1:c.905G>T	XP_011521506.1:p.Gly302Val
XM_011523205.1:c.905G>T	XP_011521507.1:p.Gly302Val
XR_243416.2:n.1650G>T
XR_429723.1:n.1639G>T
XM_011523202.2:c.1124G>T	XP_011521504.1:p.Gly375Val
XM_017023400.2:c.1631G>T	XP_016878889.1:p.Gly544Val
XM_017023401.1:c.880G>T	XP_016878890.1:p.Ala294Ser
XM_017023402.1:c.703G>T	XP_016878891.1:p.Ala235Ser
XM_024450338.1:c.905G>T	XP_024306106.1:p.Gly302Val
NM_018296.6:c.1631G>T MANE Select	NP_060766.5:p.Gly544Val
NM_001161575.2:c.1268G>T	NP_001155047.1:p.Gly423Val