Canonical Allele Identifier: CA2641296440

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23904409-CTCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23904411_23904414del , CM000680.2:g.23904411_23904414del	GRCh38
NC_000018.9:g.21484375_21484378del , CM000680.1:g.21484375_21484378del	GRCh37
NC_000018.8:g.19738373_19738376del	NCBI36
NG_007853.2:g.219814_219817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1647-142_1647-139del MANE Plus Clinical	ENSP00000269217.5:n.1647-142_1647-139del
ENST00000313654.14:c.6474-142_6474-139del MANE Select	ENSP00000324532.8:n.6474-142_6474-139del
ENST00000649721.1:c.3366-142_3366-139del	ENSP00000497885.1:n.3366-142_3366-139del
ENST00000269217.10:c.1647-142_1647-139del	ENSP00000269217.5:n.1647-142_1647-139del
ENST00000313654.13:c.6474-142_6474-139del	ENSP00000324532.8:n.6474-142_6474-139del
ENST00000399516.7:c.6306-142_6306-139del	ENSP00000382432.2:n.6306-142_6306-139del
ENST00000586751.5:c.1252-142_1252-139del
ENST00000587184.5:c.1479-142_1479-139del	ENSP00000466557.1:n.1479-142_1479-139del
ENST00000588770.5:n.1052-142_1052-139del
NM_000227.4:c.1647-142_1647-139del	NP_000218.3:n.1647-142_1647-139del
NM_001127717.2:c.6306-142_6306-139del	NP_001121189.2:n.6306-142_6306-139del
NM_001127718.2:c.1479-142_1479-139del	NP_001121190.2:n.1479-142_1479-139del
NM_198129.2:c.6474-142_6474-139del	NP_937762.2:n.6474-142_6474-139del
XM_011525978.1:c.6501-142_6501-139del	XP_011524280.1:n.6501-142_6501-139del
XM_011525979.1:c.6492-142_6492-139del	XP_011524281.1:n.6492-142_6492-139del
XM_011525980.1:c.6483-142_6483-139del	XP_011524282.1:n.6483-142_6483-139del
XM_011525981.1:c.6369-142_6369-139del	XP_011524283.1:n.6369-142_6369-139del
XM_011525982.1:c.6501-142_6501-139del	XP_011524284.1:n.6501-142_6501-139del
XM_011525978.2:c.6501-142_6501-139del	XP_011524280.1:n.6501-142_6501-139del
XM_011525979.2:c.6492-142_6492-139del	XP_011524281.1:n.6492-142_6492-139del
XM_011525980.2:c.6483-142_6483-139del	XP_011524282.1:n.6483-142_6483-139del
XM_011525981.2:c.6369-142_6369-139del	XP_011524283.1:n.6369-142_6369-139del
XM_011525982.2:c.6501-142_6501-139del	XP_011524284.1:n.6501-142_6501-139del
XM_017025743.1:c.4353-142_4353-139del	XP_016881232.1:n.4353-142_4353-139del
XM_017025744.1:c.2043-142_2043-139del	XP_016881233.1:n.2043-142_2043-139del
XR_001753199.1:n.6742-142_6742-139del
NM_000227.5:c.1647-142_1647-139del	NP_000218.3:n.1647-142_1647-139del
NM_001127717.3:c.6306-142_6306-139del	NP_001121189.2:n.6306-142_6306-139del
NM_001127718.3:c.1479-142_1479-139del	NP_001121190.2:n.1479-142_1479-139del
NM_198129.3:c.6474-142_6474-139del	NP_937762.2:n.6474-142_6474-139del
NM_000227.6:c.1647-142_1647-139del MANE Plus Clinical	NP_000218.3:n.1647-142_1647-139del
NM_001127717.4:c.6306-142_6306-139del	NP_001121189.2:n.6306-142_6306-139del
NM_001127718.4:c.1479-142_1479-139del	NP_001121190.2:n.1479-142_1479-139del
NM_198129.4:c.6474-142_6474-139del MANE Select	NP_937762.2:n.6474-142_6474-139del