Canonical Allele Identifier: CA11288481
Gene: LRRTM4 HGNC NCBI
LRRTM4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1470506
gnomAD v2: 2-77223938-C-T
gnomAD v3: 2-76996812-C-T
gnomAD v4: 2-76996812-C-T
MyVariant Identifiers: chr2:g.77223938C>T (hg19) chr2:g.76996812C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.76996812C>T , CM000664.2:g.76996812C>T GRCh38
NC_000002.11:g.77223938C>T , CM000664.1:g.77223938C>T GRCh37
NC_000002.10:g.77077446C>T NCBI36
NG_053082.1:g.530622G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000409884.6:c.1552-247896G>A (LRRTM4) MANE Select ENSP00000387297.1:n.1552-247896G>A
ENST00000409093.1:c.1552-247896G>A (LRRTM4) ENSP00000386357.1:n.1552-247896G>A
ENST00000409884.5:c.1552-247896G>A (LRRTM4) ENSP00000387297.1:n.1552-247896G>A
ENST00000409911.5:c.1555-247896G>A (LRRTM4) ENSP00000387228.1:n.1555-247896G>A
NM_001134745.1:c.1552-247896G>A (LRRTM4) NP_001128217.1:n.1552-247896G>A
NM_001282924.1:c.1552-247896G>A (LRRTM4) NP_001269853.1:n.1552-247896G>A
NR_110284.1:n.232+6886C>T (LRRTM4-AS1)
XM_011533115.1:c.1555-239027G>A (LRRTM4) XP_011531417.1:n.1555-239027G>A
XM_011533116.1:c.1552-239027G>A (LRRTM4) XP_011531418.1:n.1552-239027G>A
XM_011533117.1:c.1555-247896G>A (LRRTM4) XP_011531419.1:n.1555-247896G>A
NM_001134745.2:c.1552-247896G>A (LRRTM4) NP_001128217.1:n.1552-247896G>A
NM_001282924.2:c.1552-247896G>A (LRRTM4) NP_001269853.1:n.1552-247896G>A
NM_001330370.1:c.1555-247896G>A (LRRTM4) NP_001317299.1:n.1555-247896G>A
NR_146416.1:n.326-247896G>A (LRRTM4)
NM_001134745.3:c.1552-247896G>A (LRRTM4) MANE Select NP_001128217.1:n.1552-247896G>A
NM_001282924.3:c.1552-247896G>A (LRRTM4) NP_001269853.1:n.1552-247896G>A
NM_001330370.2:c.1555-247896G>A (LRRTM4) NP_001317299.1:n.1555-247896G>A
NR_146416.2:n.269-247896G>A (LRRTM4)
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