Canonical Allele Identifier: CA8109709

Gene: LRRC36

Linked Data

• dbSNP Id: rs143776862
• ExAC: 16:67409112 TTTTG / T
• gnomAD v2: 16-67409112-TTTTG-T
• gnomAD v3: 16-67375209-TTTTG-T
• gnomAD v4: 16-67375209-TTTTG-T
• MyVariant Identifiers: chr16:g.67409113_67409116del (hg19) ; chr16:g.67375211_67375214del (hg38) ; chr16:g.67375210_67375213del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375221_67375224del , CM000678.2:g.67375221_67375224del	GRCh38
NC_000016.9:g.67409124_67409127del , CM000678.1:g.67409124_67409127del	GRCh37
NC_000016.8:g.65966625_65966628del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1495-26_1495-23del MANE Select	ENSP00000329943.6:n.1495-26_1495-23del
ENST00000329956.10:c.1495-26_1495-23del	ENSP00000329943.6:n.1495-26_1495-23del
ENST00000435835.3:c.1132-3368_1132-3365del	ENSP00000411122.3:n.1132-3368_1132-3365del
ENST00000563189.5:c.1132-26_1132-23del	ENSP00000455103.1:n.1132-26_1132-23del
ENST00000565019.6:c.1072-94_1072-91del
ENST00000567723.5:c.*821-26_*821-23del	ENSP00000455799.1:n.*821-26_*821-23del
ENST00000567823.5:c.215-26_215-23del	ENSP00000456164.1:n.215-26_215-23del
ENST00000568010.5:c.*246-37_*246-34del	ENSP00000455018.1:n.*246-37_*246-34del
NM_001161575.1:c.1132-26_1132-23del	NP_001155047.1:n.1132-26_1132-23del
NM_018296.5:c.1495-26_1495-23del	NP_060766.5:n.1495-26_1495-23del
XM_005256025.2:c.1495-26_1495-23del	XP_005256082.1:n.1495-26_1495-23del
XM_005256026.2:c.1054-26_1054-23del	XP_005256083.1:n.1054-26_1054-23del
XM_005256027.2:c.1495-26_1495-23del	XP_005256084.1:n.1495-26_1495-23del
XM_005256028.1:c.991-26_991-23del	XP_005256085.1:n.991-26_991-23del
XM_011523199.1:c.1495-26_1495-23del	XP_011521501.1:n.1495-26_1495-23del
XM_011523200.1:c.1495-26_1495-23del	XP_011521502.1:n.1495-26_1495-23del
XM_011523201.1:c.991-26_991-23del	XP_011521503.1:n.991-26_991-23del
XM_011523202.1:c.988-26_988-23del	XP_011521504.1:n.988-26_988-23del
XM_011523203.1:c.877-26_877-23del	XP_011521505.1:n.877-26_877-23del
XM_011523204.1:c.769-26_769-23del	XP_011521506.1:n.769-26_769-23del
XM_011523205.1:c.769-26_769-23del	XP_011521507.1:n.769-26_769-23del
XR_243416.2:n.1514-26_1514-23del
XR_429723.1:n.1514-37_1514-34del
XM_011523202.2:c.988-26_988-23del	XP_011521504.1:n.988-26_988-23del
XM_017023400.2:c.1495-26_1495-23del	XP_016878889.1:n.1495-26_1495-23del
XM_017023401.1:c.755-37_755-34del	XP_016878890.1:n.755-37_755-34del
XM_017023402.1:c.578-37_578-34del	XP_016878891.1:n.578-37_578-34del
XM_024450338.1:c.769-26_769-23del	XP_024306106.1:n.769-26_769-23del
NM_018296.6:c.1495-26_1495-23del MANE Select	NP_060766.5:n.1495-26_1495-23del
NM_001161575.2:c.1132-26_1132-23del	NP_001155047.1:n.1132-26_1132-23del