Canonical Allele Identifier: CA1262698359
Gene: LRRTM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.77019205A>C , CM000664.2:g.77019205A>C GRCh38
NC_000002.11:g.77246331A>C , CM000664.1:g.77246331A>C GRCh37
NC_000002.10:g.77099839A>C NCBI36
NG_053082.1:g.508229T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000409884.6:c.1552-270289T>G MANE Select ENSP00000387297.1:n.1552-270289T>G
ENST00000409093.1:c.1552-270289T>G ENSP00000386357.1:n.1552-270289T>G
ENST00000409884.5:c.1552-270289T>G ENSP00000387297.1:n.1552-270289T>G
ENST00000409911.5:c.1555-270289T>G ENSP00000387228.1:n.1555-270289T>G
NM_001134745.1:c.1552-270289T>G NP_001128217.1:n.1552-270289T>G
NM_001282924.1:c.1552-270289T>G NP_001269853.1:n.1552-270289T>G
XM_011533115.1:c.1555-261420T>G XP_011531417.1:n.1555-261420T>G
XM_011533116.1:c.1552-261420T>G XP_011531418.1:n.1552-261420T>G
XM_011533117.1:c.1555-270289T>G XP_011531419.1:n.1555-270289T>G
NM_001134745.2:c.1552-270289T>G NP_001128217.1:n.1552-270289T>G
NM_001282924.2:c.1552-270289T>G NP_001269853.1:n.1552-270289T>G
NM_001330370.1:c.1555-270289T>G NP_001317299.1:n.1555-270289T>G
NR_146416.1:n.326-270289T>G
NM_001134745.3:c.1552-270289T>G MANE Select NP_001128217.1:n.1552-270289T>G
NM_001282924.3:c.1552-270289T>G NP_001269853.1:n.1552-270289T>G
NM_001330370.2:c.1555-270289T>G NP_001317299.1:n.1555-270289T>G
NR_146416.2:n.269-270289T>G