Canonical Allele Identifier: CA667978874

Gene: LRRC20

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.70354622T>A , CM000672.2:g.70354622T>A	GRCh38
NC_000010.10:g.72114378T>A , CM000672.1:g.72114378T>A	GRCh37
NC_000010.9:g.71784384T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000446961.4:c.83-13920A>T MANE Select	ENSP00000413745.2:n.83-13920A>T
ENST00000446961.3:c.83-13920A>T	ENSP00000413745.1:n.83-13920A>T
ENST00000355790.8:c.83-13920A>T	ENSP00000348043.4:n.83-13920A>T
ENST00000357631.6:c.83-13920A>T	ENSP00000350255.2:n.83-13920A>T
ENST00000358141.6:c.82+21830A>T	ENSP00000350860.2:n.82+21830A>T
ENST00000373224.5:c.83-13920A>T	ENSP00000362321.1:n.83-13920A>T
ENST00000395010.5:c.-125-13920A>T	ENSP00000378457.2:n.-125-13920A>T
ENST00000395011.5:c.82+21830A>T	ENSP00000378458.1:n.82+21830A>T
ENST00000446961.2:c.83-13920A>T	ENSP00000413745.1:n.83-13920A>T
NM_001278211.1:c.83-13920A>T	NP_001265140.1:n.83-13920A>T
NM_001278212.1:c.83-13920A>T	NP_001265141.1:n.83-13920A>T
NM_001278213.1:c.82+21830A>T	NP_001265142.1:n.82+21830A>T
NM_001278214.1:c.-125-13920A>T	NP_001265143.1:n.-125-13920A>T
NM_018205.3:c.83-13920A>T	NP_060675.1:n.83-13920A>T
NM_018239.3:c.82+21830A>T	NP_060709.2:n.82+21830A>T
NM_207119.2:c.83-13920A>T	NP_997002.1:n.83-13920A>T
NR_103467.1:n.102+27927A>T
NR_103468.1:n.103-13920A>T
XM_017016374.1:c.83-13920A>T	XP_016871863.1:n.83-13920A>T
XM_017016375.1:c.83-13920A>T	XP_016871864.1:n.83-13920A>T
NM_001278212.2:c.83-13920A>T MANE Select	NP_001265141.1:n.83-13920A>T
NM_001278211.2:c.83-13920A>T	NP_001265140.1:n.83-13920A>T
NM_018205.4:c.83-13920A>T	NP_060675.1:n.83-13920A>T
NM_018239.4:c.82+21830A>T	NP_060709.2:n.82+21830A>T
NM_207119.3:c.83-13920A>T	NP_997002.1:n.83-13920A>T
NR_103467.2:n.77+27927A>T
NR_103468.2:n.78-13920A>T
NM_001278213.2:c.82+21830A>T	NP_001265142.1:n.82+21830A>T
NM_001278214.2:c.-125-13920A>T	NP_001265143.1:n.-125-13920A>T