Canonical Allele Identifier: CA1140213307

Gene: LRRC7

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.69741396T= , CM000663.2:g.69741396T=	GRCh38
NC_000001.10:g.70207079T= , CM000663.1:g.70207079T=	GRCh37
NC_000001.9:g.69979667T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001370785.2:c.101-18795T= MANE Select	NP_001357714.1:n.101-18795T=
ENST00000651989.2:c.101-18795T= MANE Select	ENSP00000498937.2:n.101-18795T=
NM_001330635.1:c.2-18795T=	NP_001317564.1:n.2-18795T=
NM_001330635.3:c.2-18795T=	NP_001317564.1:n.2-18795T=
NM_001350216.1:c.104-18795T=	NP_001337145.1:n.104-18795T=
NM_001350216.2:c.104-18795T=	NP_001337145.1:n.104-18795T=
NM_001350216.3:c.104-18795T=	NP_001337145.1:n.104-18795T=
NM_001366836.1:c.101-18795T=	NP_001353765.1:n.101-18795T=
NM_001366836.3:c.101-18795T=	NP_001353765.1:n.101-18795T=
NM_001366837.1:c.2-18795T=	NP_001353766.1:n.2-18795T=
NM_001366837.3:c.2-18795T=	NP_001353766.1:n.2-18795T=
NM_001366838.1:c.101-18795T=	NP_001353767.1:n.101-18795T=
NM_001366838.3:c.101-18795T=	NP_001353767.1:n.101-18795T=
NM_001366839.1:c.2-18795T=	NP_001353768.1:n.2-18795T=
NM_001366839.3:c.2-18795T=	NP_001353768.1:n.2-18795T=
NM_001366840.1:c.104-18795T=	NP_001353769.1:n.104-18795T=
NM_001366841.1:c.2-18795T=	NP_001353770.1:n.2-18795T=
NM_001366842.1:c.158-18795T=	NP_001353771.1:n.158-18795T=
ENST00000310961.9:c.2-18795T=	ENSP00000309245.4:n.2-18795T=
ENST00000370958.5:c.101-18795T=	ENSP00000359997.1:n.101-18795T=
XM_011541836.1:c.104-18795T=	XP_011540138.1:n.104-18795T=
XM_017001885.1:c.158-18795T=	XP_016857374.1:n.158-18795T=
XM_017001886.1:c.158-18795T=	XP_016857375.1:n.158-18795T=
XM_017001887.1:c.158-18795T=	XP_016857376.1:n.158-18795T=
XM_017001888.1:c.158-18795T=	XP_016857377.1:n.158-18795T=
XM_017001889.1:c.158-18795T=	XP_016857378.1:n.158-18795T=
XM_017001892.1:c.158-18795T=	XP_016857381.1:n.158-18795T=
XM_017001895.1:c.158-18795T=	XP_016857384.1:n.158-18795T=