Canonical Allele Identifier: CA15636373
Gene: LRMDA HGNC NCBI

Linked Data

dbSNP Id: rs2043090

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.75538851A>G , CM000672.2:g.75538851A>G GRCh38
NC_000010.10:g.77298609A>G , CM000672.1:g.77298609A>G GRCh37
NC_000010.9:g.76968615A>G NCBI36
NG_042180.1:g.112206A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000611255.5:c.131+100357A>G MANE Select ENSP00000480240.1:n.131+100357A>G
ENST00000611255.4:c.131+100357A>G ENSP00000480240.1:n.131+100357A>G
NM_001305581.1:c.131+100357A>G NP_001292510.1:n.131+100357A>G
XM_011540256.1:c.131+100357A>G XP_011538558.1:n.131+100357A>G
XM_011540257.1:c.131+100357A>G XP_011538559.1:n.131+100357A>G
XM_011540258.1:c.131+100357A>G XP_011538560.1:n.131+100357A>G
XR_945833.1:n.398+100357A>G
NM_001305581.2:c.131+100357A>G MANE Select NP_001292510.1:n.131+100357A>G