Canonical Allele Identifier: CA2641292569
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23876276_23876277del , CM000680.2:g.23876276_23876277del GRCh38
NC_000018.9:g.21456240_21456241del , CM000680.1:g.21456240_21456241del GRCh37
NC_000018.8:g.19710238_19710239del NCBI36
NG_007853.2:g.191679_191680del

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.172-18_172-17del MANE Plus Clinical ENSP00000269217.5:n.172-18_172-17del
ENST00000313654.14:c.4999-18_4999-17del MANE Select ENSP00000324532.8:n.4999-18_4999-17del
ENST00000649721.1:c.1891-18_1891-17del ENSP00000497885.1:n.1891-18_1891-17del
ENST00000269217.10:c.172-18_172-17del ENSP00000269217.5:n.172-18_172-17del
ENST00000313654.13:c.4999-18_4999-17del ENSP00000324532.8:n.4999-18_4999-17del
ENST00000399516.7:c.4999-18_4999-17del ENSP00000382432.2:n.4999-18_4999-17del
ENST00000587184.5:c.172-18_172-17del ENSP00000466557.1:n.172-18_172-17del
NM_000227.4:c.172-18_172-17del NP_000218.3:n.172-18_172-17del
NM_001127717.2:c.4999-18_4999-17del NP_001121189.2:n.4999-18_4999-17del
NM_001127718.2:c.172-18_172-17del NP_001121190.2:n.172-18_172-17del
NM_198129.2:c.4999-18_4999-17del NP_937762.2:n.4999-18_4999-17del
XM_011525978.1:c.5026-18_5026-17del XP_011524280.1:n.5026-18_5026-17del
XM_011525979.1:c.5017-18_5017-17del XP_011524281.1:n.5017-18_5017-17del
XM_011525980.1:c.5008-18_5008-17del XP_011524282.1:n.5008-18_5008-17del
XM_011525981.1:c.4894-18_4894-17del XP_011524283.1:n.4894-18_4894-17del
XM_011525982.1:c.5026-18_5026-17del XP_011524284.1:n.5026-18_5026-17del
XM_011525978.2:c.5026-18_5026-17del XP_011524280.1:n.5026-18_5026-17del
XM_011525979.2:c.5017-18_5017-17del XP_011524281.1:n.5017-18_5017-17del
XM_011525980.2:c.5008-18_5008-17del XP_011524282.1:n.5008-18_5008-17del
XM_011525981.2:c.4894-18_4894-17del XP_011524283.1:n.4894-18_4894-17del
XM_011525982.2:c.5026-18_5026-17del XP_011524284.1:n.5026-18_5026-17del
XM_017025743.1:c.2878-18_2878-17del XP_016881232.1:n.2878-18_2878-17del
XM_017025744.1:c.568-18_568-17del XP_016881233.1:n.568-18_568-17del
XR_001753199.1:n.5267-18_5267-17del
NM_000227.5:c.172-18_172-17del NP_000218.3:n.172-18_172-17del
NM_001127717.3:c.4999-18_4999-17del NP_001121189.2:n.4999-18_4999-17del
NM_001127718.3:c.172-18_172-17del NP_001121190.2:n.172-18_172-17del
NM_198129.3:c.4999-18_4999-17del NP_937762.2:n.4999-18_4999-17del
NM_000227.6:c.172-18_172-17del MANE Plus Clinical NP_000218.3:n.172-18_172-17del
NM_001127717.4:c.4999-18_4999-17del NP_001121189.2:n.4999-18_4999-17del
NM_001127718.4:c.172-18_172-17del NP_001121190.2:n.172-18_172-17del
NM_198129.4:c.4999-18_4999-17del MANE Select NP_937762.2:n.4999-18_4999-17del