Canonical Allele Identifier: CA2578736676
Gene: LAMA2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129192599del , CM000668.2:g.129192599del GRCh38
NC_000006.11:g.129513744del , CM000668.1:g.129513744del GRCh37
NC_000006.10:g.129555437del NCBI36
NG_008678.1:g.314459del , LRG_409:g.314459del

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.1609-81del ENSP00000481744.2:n.1609-81del
ENST00000618192.5:c.1609-81del ENSP00000480802.2:n.1609-81del
ENST00000686599.1:n.1714-81del
ENST00000690881.1:n.1072-81del
ENST00000421865.3:c.1609-81del MANE Select ENSP00000400365.2:n.1609-81del
ENST00000421865.2:c.1609-81del ENSP00000400365.2:n.1609-81del
ENST00000617695.4:c.1609-81del ENSP00000481744.1:n.1609-81del
ENST00000618192.4:c.1609-81del ENSP00000480802.1:n.1609-81del
NM_000426.3:c.1609-81del , LRG_409t1:c.1609-81del NP_000417.2:n.1609-81del
NM_001079823.1:c.1609-81del NP_001073291.1:n.1609-81del
XM_005266981.2:c.1609-81del XP_005267038.1:n.1609-81del
XM_005266982.2:c.1609-81del XP_005267039.1:n.1609-81del
XM_011535820.1:c.1609-81del XP_011534122.1:n.1609-81del
XM_005266981.3:c.1609-81del XP_005267038.1:n.1609-81del
XM_005266982.3:c.1609-81del XP_005267039.1:n.1609-81del
XM_011535820.2:c.1609-81del XP_011534122.1:n.1609-81del
XM_017010851.2:c.1615-81del XP_016866340.1:n.1615-81del
XM_017010853.1:c.1609-81del XP_016866342.1:n.1609-81del
NM_000426.4:c.1609-81del MANE Select NP_000417.3:n.1609-81del
NM_001079823.2:c.1609-81del NP_001073291.2:n.1609-81del