Canonical Allele Identifier: CA2739268591

Gene: LAMA3

Linked Data

• ClinVar Variation Id: 2786838
• ClinVar RCV Id: RCV003660402

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23902990T>A , CM000680.2:g.23902990T>A	GRCh38
NC_000018.9:g.21482954T>A , CM000680.1:g.21482954T>A	GRCh37
NC_000018.8:g.19736952T>A	NCBI36
NG_007853.2:g.218393T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.1375-19T>A MANE Plus Clinical	ENSP00000269217.5:n.1375-19T>A
ENST00000313654.14:c.6202-19T>A MANE Select	ENSP00000324532.8:n.6202-19T>A
ENST00000649721.1:c.3094-19T>A	ENSP00000497885.1:n.3094-19T>A
ENST00000269217.10:c.1375-19T>A	ENSP00000269217.5:n.1375-19T>A
ENST00000313654.13:c.6202-19T>A	ENSP00000324532.8:n.6202-19T>A
ENST00000399516.7:c.6034-19T>A	ENSP00000382432.2:n.6034-19T>A
ENST00000586751.5:c.980-19T>A
ENST00000587184.5:c.1207-19T>A	ENSP00000466557.1:n.1207-19T>A
ENST00000588770.5:n.780-19T>A
NM_000227.4:c.1375-19T>A	NP_000218.3:n.1375-19T>A
NM_001127717.2:c.6034-19T>A	NP_001121189.2:n.6034-19T>A
NM_001127718.2:c.1207-19T>A	NP_001121190.2:n.1207-19T>A
NM_198129.2:c.6202-19T>A	NP_937762.2:n.6202-19T>A
XM_011525978.1:c.6229-19T>A	XP_011524280.1:n.6229-19T>A
XM_011525979.1:c.6220-19T>A	XP_011524281.1:n.6220-19T>A
XM_011525980.1:c.6211-19T>A	XP_011524282.1:n.6211-19T>A
XM_011525981.1:c.6097-19T>A	XP_011524283.1:n.6097-19T>A
XM_011525982.1:c.6229-19T>A	XP_011524284.1:n.6229-19T>A
XM_011525978.2:c.6229-19T>A	XP_011524280.1:n.6229-19T>A
XM_011525979.2:c.6220-19T>A	XP_011524281.1:n.6220-19T>A
XM_011525980.2:c.6211-19T>A	XP_011524282.1:n.6211-19T>A
XM_011525981.2:c.6097-19T>A	XP_011524283.1:n.6097-19T>A
XM_011525982.2:c.6229-19T>A	XP_011524284.1:n.6229-19T>A
XM_017025743.1:c.4081-19T>A	XP_016881232.1:n.4081-19T>A
XM_017025744.1:c.1771-19T>A	XP_016881233.1:n.1771-19T>A
XR_001753199.1:n.6470-19T>A
NM_000227.5:c.1375-19T>A	NP_000218.3:n.1375-19T>A
NM_001127717.3:c.6034-19T>A	NP_001121189.2:n.6034-19T>A
NM_001127718.3:c.1207-19T>A	NP_001121190.2:n.1207-19T>A
NM_198129.3:c.6202-19T>A	NP_937762.2:n.6202-19T>A
NM_000227.6:c.1375-19T>A MANE Plus Clinical	NP_000218.3:n.1375-19T>A
NM_001127717.4:c.6034-19T>A	NP_001121189.2:n.6034-19T>A
NM_001127718.4:c.1207-19T>A	NP_001121190.2:n.1207-19T>A
NM_198129.4:c.6202-19T>A MANE Select	NP_937762.2:n.6202-19T>A