Canonical Allele Identifier: CA2576472886

Gene: LAMA3

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23904508_23904511del , CM000680.2:g.23904508_23904511del	GRCh38
NC_000018.9:g.21484472_21484475del , CM000680.1:g.21484472_21484475del	GRCh37
NC_000018.8:g.19738470_19738473del	NCBI36
NG_007853.2:g.219911_219914del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1647-45_1647-42del MANE Plus Clinical	ENSP00000269217.5:n.1647-45_1647-42del
ENST00000313654.14:c.6474-45_6474-42del MANE Select	ENSP00000324532.8:n.6474-45_6474-42del
ENST00000649721.1:c.3366-45_3366-42del	ENSP00000497885.1:n.3366-45_3366-42del
ENST00000269217.10:c.1647-45_1647-42del	ENSP00000269217.5:n.1647-45_1647-42del
ENST00000313654.13:c.6474-45_6474-42del	ENSP00000324532.8:n.6474-45_6474-42del
ENST00000399516.7:c.6306-45_6306-42del	ENSP00000382432.2:n.6306-45_6306-42del
ENST00000586751.5:c.1252-45_1252-42del
ENST00000587184.5:c.1479-45_1479-42del	ENSP00000466557.1:n.1479-45_1479-42del
ENST00000588770.5:n.1052-45_1052-42del
NM_000227.4:c.1647-45_1647-42del	NP_000218.3:n.1647-45_1647-42del
NM_001127717.2:c.6306-45_6306-42del	NP_001121189.2:n.6306-45_6306-42del
NM_001127718.2:c.1479-45_1479-42del	NP_001121190.2:n.1479-45_1479-42del
NM_198129.2:c.6474-45_6474-42del	NP_937762.2:n.6474-45_6474-42del
XM_011525978.1:c.6501-45_6501-42del	XP_011524280.1:n.6501-45_6501-42del
XM_011525979.1:c.6492-45_6492-42del	XP_011524281.1:n.6492-45_6492-42del
XM_011525980.1:c.6483-45_6483-42del	XP_011524282.1:n.6483-45_6483-42del
XM_011525981.1:c.6369-45_6369-42del	XP_011524283.1:n.6369-45_6369-42del
XM_011525982.1:c.6501-45_6501-42del	XP_011524284.1:n.6501-45_6501-42del
XM_011525978.2:c.6501-45_6501-42del	XP_011524280.1:n.6501-45_6501-42del
XM_011525979.2:c.6492-45_6492-42del	XP_011524281.1:n.6492-45_6492-42del
XM_011525980.2:c.6483-45_6483-42del	XP_011524282.1:n.6483-45_6483-42del
XM_011525981.2:c.6369-45_6369-42del	XP_011524283.1:n.6369-45_6369-42del
XM_011525982.2:c.6501-45_6501-42del	XP_011524284.1:n.6501-45_6501-42del
XM_017025743.1:c.4353-45_4353-42del	XP_016881232.1:n.4353-45_4353-42del
XM_017025744.1:c.2043-45_2043-42del	XP_016881233.1:n.2043-45_2043-42del
XR_001753199.1:n.6742-45_6742-42del
NM_000227.5:c.1647-45_1647-42del	NP_000218.3:n.1647-45_1647-42del
NM_001127717.3:c.6306-45_6306-42del	NP_001121189.2:n.6306-45_6306-42del
NM_001127718.3:c.1479-45_1479-42del	NP_001121190.2:n.1479-45_1479-42del
NM_198129.3:c.6474-45_6474-42del	NP_937762.2:n.6474-45_6474-42del
NM_000227.6:c.1647-45_1647-42del MANE Plus Clinical	NP_000218.3:n.1647-45_1647-42del
NM_001127717.4:c.6306-45_6306-42del	NP_001121189.2:n.6306-45_6306-42del
NM_001127718.4:c.1479-45_1479-42del	NP_001121190.2:n.1479-45_1479-42del
NM_198129.4:c.6474-45_6474-42del MANE Select	NP_937762.2:n.6474-45_6474-42del