Canonical Allele Identifier: CA2641292194
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23864914_23864923del , CM000680.2:g.23864914_23864923del GRCh38
NC_000018.9:g.21444878_21444887del , CM000680.1:g.21444878_21444887del GRCh37
NC_000018.8:g.19698876_19698885del NCBI36
NG_007853.2:g.180317_180326del

Transcript Alleles

HGVS Amino-acid Change
ENST00000313654.14:c.4683+31_4683+40del MANE Select ENSP00000324532.8:n.4683+31_4683+40del
ENST00000649721.1:c.1575+31_1575+40del ENSP00000497885.1:n.1575+31_1575+40del
ENST00000313654.13:c.4683+31_4683+40del ENSP00000324532.8:n.4683+31_4683+40del
ENST00000399516.7:c.4683+31_4683+40del ENSP00000382432.2:n.4683+31_4683+40del
NM_001127717.2:c.4683+31_4683+40del NP_001121189.2:n.4683+31_4683+40del
NM_198129.2:c.4683+31_4683+40del NP_937762.2:n.4683+31_4683+40del
XM_011525978.1:c.4710+31_4710+40del XP_011524280.1:n.4710+31_4710+40del
XM_011525979.1:c.4701+31_4701+40del XP_011524281.1:n.4701+31_4701+40del
XM_011525980.1:c.4692+31_4692+40del XP_011524282.1:n.4692+31_4692+40del
XM_011525981.1:c.4578+31_4578+40del XP_011524283.1:n.4578+31_4578+40del
XM_011525982.1:c.4710+31_4710+40del XP_011524284.1:n.4710+31_4710+40del
XM_011525978.2:c.4710+31_4710+40del XP_011524280.1:n.4710+31_4710+40del
XM_011525979.2:c.4701+31_4701+40del XP_011524281.1:n.4701+31_4701+40del
XM_011525980.2:c.4692+31_4692+40del XP_011524282.1:n.4692+31_4692+40del
XM_011525981.2:c.4578+31_4578+40del XP_011524283.1:n.4578+31_4578+40del
XM_011525982.2:c.4710+31_4710+40del XP_011524284.1:n.4710+31_4710+40del
XM_017025743.1:c.2562+31_2562+40del XP_016881232.1:n.2562+31_2562+40del
XM_017025744.1:c.252+31_252+40del XP_016881233.1:n.252+31_252+40del
XR_001753199.1:n.4951+31_4951+40del
NM_001127717.3:c.4683+31_4683+40del NP_001121189.2:n.4683+31_4683+40del
NM_198129.3:c.4683+31_4683+40del NP_937762.2:n.4683+31_4683+40del
NM_001127717.4:c.4683+31_4683+40del NP_001121189.2:n.4683+31_4683+40del
NM_198129.4:c.4683+31_4683+40del MANE Select NP_937762.2:n.4683+31_4683+40del