Canonical Allele Identifier: CA570051710
Gene: LAMA2 HGNC NCBI

Linked Data

dbSNP Id: rs1256493661

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129297897_129297910del , CM000668.2:g.129297897_129297910del GRCh38
NC_000006.11:g.129619042_129619055del , CM000668.1:g.129619042_129619055del GRCh37
NC_000006.10:g.129660735_129660748del NCBI36
NG_008678.1:g.419757_419770del , LRG_409:g.419757_419770del

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.3037+32_3037+45del ENSP00000481744.2:n.3037+32_3037+45del
ENST00000618192.5:c.3301+32_3301+45del ENSP00000480802.2:n.3301+32_3301+45del
ENST00000421865.3:c.3037+32_3037+45del MANE Select ENSP00000400365.2:n.3037+32_3037+45del
ENST00000421865.2:c.3037+32_3037+45del ENSP00000400365.2:n.3037+32_3037+45del
ENST00000617695.4:c.3037+32_3037+45del ENSP00000481744.1:n.3037+32_3037+45del
ENST00000618192.4:c.3037+32_3037+45del ENSP00000480802.1:n.3037+32_3037+45del
NM_000426.3:c.3037+32_3037+45del , LRG_409t1:c.3037+32_3037+45del NP_000417.2:n.3037+32_3037+45del
NM_001079823.1:c.3037+32_3037+45del NP_001073291.1:n.3037+32_3037+45del
XM_005266981.2:c.3301+32_3301+45del XP_005267038.1:n.3301+32_3301+45del
XM_005266982.2:c.3301+32_3301+45del XP_005267039.1:n.3301+32_3301+45del
XM_011535820.1:c.3301+32_3301+45del XP_011534122.1:n.3301+32_3301+45del
XM_005266981.3:c.3301+32_3301+45del XP_005267038.1:n.3301+32_3301+45del
XM_005266982.3:c.3301+32_3301+45del XP_005267039.1:n.3301+32_3301+45del
XM_011535820.2:c.3301+32_3301+45del XP_011534122.1:n.3301+32_3301+45del
XM_017010851.2:c.3307+32_3307+45del XP_016866340.1:n.3307+32_3307+45del
XM_017010852.1:c.1432+32_1432+45del XP_016866341.1:n.1432+32_1432+45del
XM_017010853.1:c.3301+32_3301+45del XP_016866342.1:n.3301+32_3301+45del
NM_000426.4:c.3037+32_3037+45del MANE Select NP_000417.3:n.3037+32_3037+45del
NM_001079823.2:c.3037+32_3037+45del NP_001073291.2:n.3037+32_3037+45del