Canonical Allele Identifier: CA818836775
Gene: LAMA2 HGNC NCBI

Linked Data

dbSNP Id: rs1371950112

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129342195_129342196del , CM000668.2:g.129342195_129342196del GRCh38
NC_000006.11:g.129663340_129663341del , CM000668.1:g.129663340_129663341del GRCh37
NC_000006.10:g.129705033_129705034del NCBI36
NG_008678.1:g.464055_464056del , LRG_409:g.464055_464056del

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.4312-148_4312-147del ENSP00000481744.2:n.4312-148_4312-147del
ENST00000618192.5:c.4576-148_4576-147del ENSP00000480802.2:n.4576-148_4576-147del
ENST00000421865.3:c.4312-148_4312-147del MANE Select ENSP00000400365.2:n.4312-148_4312-147del
ENST00000421865.2:c.4312-148_4312-147del ENSP00000400365.2:n.4312-148_4312-147del
ENST00000617695.4:c.4312-148_4312-147del ENSP00000481744.1:n.4312-148_4312-147del
ENST00000618192.4:c.4312-148_4312-147del ENSP00000480802.1:n.4312-148_4312-147del
NM_000426.3:c.4312-148_4312-147del , LRG_409t1:c.4312-148_4312-147del NP_000417.2:n.4312-148_4312-147del
NM_001079823.1:c.4312-148_4312-147del NP_001073291.1:n.4312-148_4312-147del
XM_005266981.2:c.4576-148_4576-147del XP_005267038.1:n.4576-148_4576-147del
XM_005266982.2:c.4576-148_4576-147del XP_005267039.1:n.4576-148_4576-147del
XM_011535820.1:c.4576-148_4576-147del XP_011534122.1:n.4576-148_4576-147del
XM_005266981.3:c.4576-148_4576-147del XP_005267038.1:n.4576-148_4576-147del
XM_005266982.3:c.4576-148_4576-147del XP_005267039.1:n.4576-148_4576-147del
XM_011535820.2:c.4576-148_4576-147del XP_011534122.1:n.4576-148_4576-147del
XM_017010851.2:c.4582-148_4582-147del XP_016866340.1:n.4582-148_4582-147del
XM_017010852.1:c.2707-148_2707-147del XP_016866341.1:n.2707-148_2707-147del
XM_017010853.1:c.4576-148_4576-147del XP_016866342.1:n.4576-148_4576-147del
NM_000426.4:c.4312-148_4312-147del MANE Select NP_000417.3:n.4312-148_4312-147del
NM_001079823.2:c.4312-148_4312-147del NP_001073291.2:n.4312-148_4312-147del