Canonical Allele Identifier: CA11427659

Gene: LRRC31

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.169862183G>A , CM000665.2:g.169862183G>A	GRCh38
NC_000003.11:g.169579971G>A , CM000665.1:g.169579971G>A	GRCh37
NC_000003.10:g.171062665G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316428.10:c.176-370C>T MANE Select	ENSP00000325978.5:n.176-370C>T
ENST00000264676.9:c.176-370C>T	ENSP00000264676.5:n.176-370C>T
ENST00000316428.9:c.176-370C>T	ENSP00000325978.5:n.176-370C>T
ENST00000397805.2:n.243-370C>T
ENST00000523069.1:c.176-370C>T	ENSP00000429145.1:n.176-370C>T
NM_001277127.1:c.176-370C>T	NP_001264056.1:n.176-370C>T
NM_001277128.1:c.176-370C>T	NP_001264057.1:n.176-370C>T
NM_024727.3:c.176-370C>T	NP_079003.2:n.176-370C>T
XM_011513158.1:c.176-370C>T	XP_011511460.1:n.176-370C>T
XM_011513159.1:c.176-370C>T	XP_011511461.1:n.176-370C>T
XM_011513160.1:c.176-370C>T	XP_011511462.1:n.176-370C>T
XM_011513158.2:c.176-370C>T	XP_011511460.1:n.176-370C>T
XM_011513159.2:c.176-370C>T	XP_011511461.1:n.176-370C>T
XM_011513160.3:c.176-370C>T	XP_011511462.1:n.176-370C>T
XM_017007204.1:c.-20-370C>T	XP_016862693.1:n.-20-370C>T
NM_001277127.2:c.176-370C>T	NP_001264056.1:n.176-370C>T
NM_001277128.2:c.176-370C>T	NP_001264057.1:n.176-370C>T
NM_024727.4:c.176-370C>T MANE Select	NP_079003.2:n.176-370C>T