Canonical Allele Identifier: CA1419639596
Gene: LRRC31 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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