Canonical Allele Identifier: CA50781467

Gene: LRRTM4

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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