Canonical Allele Identifier: CA495962028

Gene: LRRC36

Linked Data

• gnomAD v4: 16-67375321-C-T
• MyVariant Identifiers: chr16:g.67409224C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375321C>T , CM000678.2:g.67375321C>T	GRCh38
NC_000016.9:g.67409224C>T , CM000678.1:g.67409224C>T	GRCh37
NC_000016.8:g.65966725C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1569C>T MANE Select	ENSP00000329943.6:p.Pro523=
ENST00000329956.10:c.1569C>T	ENSP00000329943.6:p.Pro523=
ENST00000435835.3:c.1132-3268C>T	ENSP00000411122.3:n.1132-3268C>T
ENST00000563189.5:c.1206C>T	ENSP00000455103.1:p.Pro402=
ENST00000565019.6:c.1078C>T
ENST00000567723.5:c.*895C>T	ENSP00000455799.1:n.*895C>T
ENST00000567823.5:c.*64C>T	ENSP00000456164.1:n.*64C>T
ENST00000568010.5:c.*309C>T	ENSP00000455018.1:n.*309C>T
NM_001161575.1:c.1206C>T	NP_001155047.1:p.Pro402=
NM_018296.5:c.1569C>T	NP_060766.5:p.Pro523=
XM_005256025.2:c.1569C>T	XP_005256082.1:p.Pro523=
XM_005256026.2:c.1128C>T	XP_005256083.1:p.Pro376=
XM_005256027.2:c.1569C>T	XP_005256084.1:p.Pro523=
XM_005256028.1:c.1065C>T	XP_005256085.1:p.Pro355=
XM_011523199.1:c.1569C>T	XP_011521501.1:p.Pro523=
XM_011523200.1:c.1569C>T	XP_011521502.1:p.Pro523=
XM_011523201.1:c.1065C>T	XP_011521503.1:p.Pro355=
XM_011523202.1:c.1062C>T	XP_011521504.1:p.Pro354=
XM_011523203.1:c.951C>T	XP_011521505.1:p.Pro317=
XM_011523204.1:c.843C>T	XP_011521506.1:p.Pro281=
XM_011523205.1:c.843C>T	XP_011521507.1:p.Pro281=
XR_243416.2:n.1588C>T
XR_429723.1:n.1577C>T
XM_011523202.2:c.1062C>T	XP_011521504.1:p.Pro354=
XM_017023400.2:c.1569C>T	XP_016878889.1:p.Pro523=
XM_017023401.1:c.818C>T	XP_016878890.1:p.Pro273Leu
XM_017023402.1:c.641C>T	XP_016878891.1:p.Pro214Leu
XM_024450338.1:c.843C>T	XP_024306106.1:p.Pro281=
NM_018296.6:c.1569C>T MANE Select	NP_060766.5:p.Pro523=
NM_001161575.2:c.1206C>T	NP_001155047.1:p.Pro402=