Canonical Allele Identifier: CA2555856244
Gene: LAMA2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129192586del , CM000668.2:g.129192586del GRCh38
NC_000006.11:g.129513731del , CM000668.1:g.129513731del GRCh37
NC_000006.10:g.129555424del NCBI36
NG_008678.1:g.314446del , LRG_409:g.314446del

Transcript Alleles

HGVS Amino-acid change
ENST00000617695.5:c.1609-94del ENSP00000481744.2:n.1609-94del
ENST00000618192.5:c.1609-94del ENSP00000480802.2:n.1609-94del
ENST00000686599.1:n.1714-94del
ENST00000690881.1:n.1072-94del
ENST00000421865.3:c.1609-94del MANE Select ENSP00000400365.2:n.1609-94del
ENST00000421865.2:c.1609-94del ENSP00000400365.2:n.1609-94del
ENST00000617695.4:c.1609-94del ENSP00000481744.1:n.1609-94del
ENST00000618192.4:c.1609-94del ENSP00000480802.1:n.1609-94del
NM_000426.3:c.1609-94del , LRG_409t1:c.1609-94del NP_000417.2:n.1609-94del
NM_001079823.1:c.1609-94del NP_001073291.1:n.1609-94del
XM_005266981.2:c.1609-94del XP_005267038.1:n.1609-94del
XM_005266982.2:c.1609-94del XP_005267039.1:n.1609-94del
XM_011535820.1:c.1609-94del XP_011534122.1:n.1609-94del
XM_005266981.3:c.1609-94del XP_005267038.1:n.1609-94del
XM_005266982.3:c.1609-94del XP_005267039.1:n.1609-94del
XM_011535820.2:c.1609-94del XP_011534122.1:n.1609-94del
XM_017010851.2:c.1615-94del XP_016866340.1:n.1615-94del
XM_017010853.1:c.1609-94del XP_016866342.1:n.1609-94del
NM_000426.4:c.1609-94del MANE Select NP_000417.3:n.1609-94del
NM_001079823.2:c.1609-94del NP_001073291.2:n.1609-94del