Canonical Allele Identifier: CA818867725
Gene: LAMA2 HGNC NCBI

Linked Data

dbSNP Id: rs1342554747

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129515939del , CM000668.2:g.129515939del GRCh38
NC_000006.11:g.129837084del , CM000668.1:g.129837084del GRCh37
NC_000006.10:g.129878777del NCBI36
NG_008678.1:g.637799del , LRG_409:g.637799del

Transcript Alleles

HGVS Amino-acid Change
ENST00000494137.2:c.1277-251del ENSP00000510626.1:n.1277-251del
ENST00000498257.6:c.1277-251del ENSP00000510533.1:n.1277-251del
ENST00000617695.5:c.9200-251del ENSP00000481744.2:n.9200-251del
ENST00000618192.5:c.9476-251del ENSP00000480802.2:n.9476-251del
ENST00000688198.1:n.2190-251del
ENST00000688799.1:c.1277-251del ENSP00000508458.1:n.1277-251del
ENST00000690858.1:n.4085-251del
ENST00000693461.1:n.1549-251del
ENST00000421865.3:c.9212-251del MANE Select ENSP00000400365.2:n.9212-251del
ENST00000421865.2:c.9212-251del ENSP00000400365.2:n.9212-251del
ENST00000617695.4:c.9200-251del ENSP00000481744.1:n.9200-251del
ENST00000618192.4:c.9209-251del ENSP00000480802.1:n.9209-251del
NM_000426.3:c.9212-251del , LRG_409t1:c.9212-251del NP_000417.2:n.9212-251del
NM_001079823.1:c.9200-251del NP_001073291.1:n.9200-251del
XM_005266981.2:c.9476-251del XP_005267038.1:n.9476-251del
XM_005266982.2:c.9464-251del XP_005267039.1:n.9464-251del
XM_011535820.1:c.9470-251del XP_011534122.1:n.9470-251del
XR_942984.1:n.1460+6538del
XR_942985.1:n.1324+6538del
XM_005266981.3:c.9476-251del XP_005267038.1:n.9476-251del
XM_005266982.3:c.9464-251del XP_005267039.1:n.9464-251del
XM_011535820.2:c.9470-251del XP_011534122.1:n.9470-251del
XM_017010851.2:c.9482-251del XP_016866340.1:n.9482-251del
XM_017010852.1:c.7607-251del XP_016866341.1:n.7607-251del
XR_001743859.1:n.3900+6538del
XR_001743860.1:n.1179+6538del
XR_001743861.1:n.1346+6538del
XR_001743863.1:n.883-13148del
XR_002956395.1:n.9131+6538del
XR_002956396.1:n.3126+6538del
NM_000426.4:c.9212-251del MANE Select NP_000417.3:n.9212-251del
NM_001079823.2:c.9200-251del NP_001073291.2:n.9200-251del