Canonical Allele Identifier: CA2576473276

Gene: LAMA3

Linked Data

• gnomAD v4: 18-23921623-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23921623G>A , CM000680.2:g.23921623G>A	GRCh38
NC_000018.9:g.21501587G>A , CM000680.1:g.21501587G>A	GRCh37
NC_000018.8:g.19755585G>A	NCBI36
NG_007853.2:g.237026G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3350+38G>A MANE Plus Clinical	ENSP00000269217.5:n.3350+38G>A
ENST00000313654.14:c.8177+38G>A MANE Select	ENSP00000324532.8:n.8177+38G>A
ENST00000649721.1:c.4772+38G>A	ENSP00000497885.1:n.4772+38G>A
ENST00000269217.10:c.3350+38G>A	ENSP00000269217.5:n.3350+38G>A
ENST00000313654.13:c.8177+38G>A	ENSP00000324532.8:n.8177+38G>A
ENST00000399516.7:c.8009+38G>A	ENSP00000382432.2:n.8009+38G>A
ENST00000586751.5:c.2955+38G>A
ENST00000587184.5:c.3182+38G>A	ENSP00000466557.1:n.3182+38G>A
ENST00000588770.5:n.2755+38G>A
NM_000227.4:c.3350+38G>A	NP_000218.3:n.3350+38G>A
NM_001127717.2:c.8009+38G>A	NP_001121189.2:n.8009+38G>A
NM_001127718.2:c.3182+38G>A	NP_001121190.2:n.3182+38G>A
NM_198129.2:c.8177+38G>A	NP_937762.2:n.8177+38G>A
XM_011525978.1:c.8204+38G>A	XP_011524280.1:n.8204+38G>A
XM_011525979.1:c.8195+38G>A	XP_011524281.1:n.8195+38G>A
XM_011525980.1:c.8186+38G>A	XP_011524282.1:n.8186+38G>A
XM_011525981.1:c.8072+38G>A	XP_011524283.1:n.8072+38G>A
XM_011525982.1:c.7907+38G>A	XP_011524284.1:n.7907+38G>A
XM_011525978.2:c.8204+38G>A	XP_011524280.1:n.8204+38G>A
XM_011525979.2:c.8195+38G>A	XP_011524281.1:n.8195+38G>A
XM_011525980.2:c.8186+38G>A	XP_011524282.1:n.8186+38G>A
XM_011525981.2:c.8072+38G>A	XP_011524283.1:n.8072+38G>A
XM_011525982.2:c.7907+38G>A	XP_011524284.1:n.7907+38G>A
XM_017025743.1:c.6056+38G>A	XP_016881232.1:n.6056+38G>A
XM_017025744.1:c.3746+38G>A	XP_016881233.1:n.3746+38G>A
XR_001753199.1:n.8445+38G>A
NM_000227.5:c.3350+38G>A	NP_000218.3:n.3350+38G>A
NM_001127717.3:c.8009+38G>A	NP_001121189.2:n.8009+38G>A
NM_001127718.3:c.3182+38G>A	NP_001121190.2:n.3182+38G>A
NM_198129.3:c.8177+38G>A	NP_937762.2:n.8177+38G>A
NM_000227.6:c.3350+38G>A MANE Plus Clinical	NP_000218.3:n.3350+38G>A
NM_001127717.4:c.8009+38G>A	NP_001121189.2:n.8009+38G>A
NM_001127718.4:c.3182+38G>A	NP_001121190.2:n.3182+38G>A
NM_198129.4:c.8177+38G>A MANE Select	NP_937762.2:n.8177+38G>A