Canonical Allele Identifier: CA11018473

Gene: LRRTM4

Linked Data

• dbSNP Id: rs2178574
• gnomAD v2: 2-77152610-A-G
• gnomAD v3: 2-76925484-A-G
• gnomAD v4: 2-76925484-A-G
• MyVariant Identifiers: chr2:g.77152610A>G (hg19) ; chr2:g.76925484A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.76925484A>G , CM000664.2:g.76925484A>G	GRCh38
NC_000002.11:g.77152610A>G , CM000664.1:g.77152610A>G	GRCh37
NC_000002.10:g.77006118A>G	NCBI36
NG_053082.1:g.601950T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000409884.6:c.1552-176568T>C MANE Select	ENSP00000387297.1:n.1552-176568T>C
ENST00000409093.1:c.1552-176568T>C	ENSP00000386357.1:n.1552-176568T>C
ENST00000409884.5:c.1552-176568T>C	ENSP00000387297.1:n.1552-176568T>C
ENST00000409911.5:c.1555-176568T>C	ENSP00000387228.1:n.1555-176568T>C
NM_001134745.1:c.1552-176568T>C	NP_001128217.1:n.1552-176568T>C
NM_001282924.1:c.1552-176568T>C	NP_001269853.1:n.1552-176568T>C
XM_011533115.1:c.1555-167699T>C	XP_011531417.1:n.1555-167699T>C
XM_011533116.1:c.1552-167699T>C	XP_011531418.1:n.1552-167699T>C
XM_011533117.1:c.1555-176568T>C	XP_011531419.1:n.1555-176568T>C
NM_001134745.2:c.1552-176568T>C	NP_001128217.1:n.1552-176568T>C
NM_001282924.2:c.1552-176568T>C	NP_001269853.1:n.1552-176568T>C
NM_001330370.1:c.1555-176568T>C	NP_001317299.1:n.1555-176568T>C
NR_146416.1:n.326-176568T>C
NM_001134745.3:c.1552-176568T>C MANE Select	NP_001128217.1:n.1552-176568T>C
NM_001282924.3:c.1552-176568T>C	NP_001269853.1:n.1552-176568T>C
NM_001330370.2:c.1555-176568T>C	NP_001317299.1:n.1555-176568T>C
NR_146416.2:n.269-176568T>C