Canonical Allele Identifier: CA396267876

Gene: LRRC36

Linked Data

• MyVariant Identifiers: chr16:g.67409171A>T (hg19) ; chr16:g.67375268A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67375268A>T , CM000678.2:g.67375268A>T	GRCh38
NC_000016.9:g.67409171A>T , CM000678.1:g.67409171A>T	GRCh37
NC_000016.8:g.65966672A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000329956.11:c.1516A>T MANE Select	ENSP00000329943.6:p.Ser506Cys
ENST00000329956.10:c.1516A>T	ENSP00000329943.6:p.Ser506Cys
ENST00000435835.3:c.1132-3321A>T	ENSP00000411122.3:n.1132-3321A>T
ENST00000563189.5:c.1153A>T	ENSP00000455103.1:p.Ser385Cys
ENST00000565019.6:c.1072-47A>T
ENST00000567723.5:c.*842A>T	ENSP00000455799.1:n.*842A>T
ENST00000567823.5:c.*11A>T	ENSP00000456164.1:n.*11A>T
ENST00000568010.5:c.*256A>T	ENSP00000455018.1:n.*256A>T
NM_001161575.1:c.1153A>T	NP_001155047.1:p.Ser385Cys
NM_018296.5:c.1516A>T	NP_060766.5:p.Ser506Cys
XM_005256025.2:c.1516A>T	XP_005256082.1:p.Ser506Cys
XM_005256026.2:c.1075A>T	XP_005256083.1:p.Ser359Cys
XM_005256027.2:c.1516A>T	XP_005256084.1:p.Ser506Cys
XM_005256028.1:c.1012A>T	XP_005256085.1:p.Ser338Cys
XM_011523199.1:c.1516A>T	XP_011521501.1:p.Ser506Cys
XM_011523200.1:c.1516A>T	XP_011521502.1:p.Ser506Cys
XM_011523201.1:c.1012A>T	XP_011521503.1:p.Ser338Cys
XM_011523202.1:c.1009A>T	XP_011521504.1:p.Ser337Cys
XM_011523203.1:c.898A>T	XP_011521505.1:p.Ser300Cys
XM_011523204.1:c.790A>T	XP_011521506.1:p.Ser264Cys
XM_011523205.1:c.790A>T	XP_011521507.1:p.Ser264Cys
XR_243416.2:n.1535A>T
XR_429723.1:n.1524A>T
XM_011523202.2:c.1009A>T	XP_011521504.1:p.Ser337Cys
XM_017023400.2:c.1516A>T	XP_016878889.1:p.Ser506Cys
XM_017023401.1:c.765A>T	XP_016878890.1:p.Val255=
XM_017023402.1:c.588A>T	XP_016878891.1:p.Val196=
XM_024450338.1:c.790A>T	XP_024306106.1:p.Ser264Cys
NM_018296.6:c.1516A>T MANE Select	NP_060766.5:p.Ser506Cys
NM_001161575.2:c.1153A>T	NP_001155047.1:p.Ser385Cys