Canonical Allele Identifier: CA402059305

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21495349T>A (hg19) ; chr18:g.23915385T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23915385T>A , CM000680.2:g.23915385T>A	GRCh38
NC_000018.9:g.21495349T>A , CM000680.1:g.21495349T>A	GRCh37
NC_000018.8:g.19749347T>A	NCBI36
NG_007853.2:g.230788T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.2914T>A MANE Plus Clinical	ENSP00000269217.5:p.Phe972Ile
ENST00000313654.14:c.7741T>A MANE Select	ENSP00000324532.8:p.Phe2581Ile
ENST00000649721.1:c.4336T>A	ENSP00000497885.1:p.Phe1446Ile
ENST00000269217.10:c.2914T>A	ENSP00000269217.5:p.Phe972Ile
ENST00000313654.13:c.7741T>A	ENSP00000324532.8:p.Phe2581Ile
ENST00000399516.7:c.7573T>A	ENSP00000382432.2:p.Phe2525Ile
ENST00000586751.5:c.2519T>A
ENST00000587184.5:c.2746T>A	ENSP00000466557.1:p.Phe916Ile
ENST00000588770.5:n.2319T>A
NM_000227.4:c.2914T>A	NP_000218.3:p.Phe972Ile
NM_001127717.2:c.7573T>A	NP_001121189.2:p.Phe2525Ile
NM_001127718.2:c.2746T>A	NP_001121190.2:p.Phe916Ile
NM_198129.2:c.7741T>A	NP_937762.2:p.Phe2581Ile
XM_011525978.1:c.7768T>A	XP_011524280.1:p.Phe2590Ile
XM_011525979.1:c.7759T>A	XP_011524281.1:p.Phe2587Ile
XM_011525980.1:c.7750T>A	XP_011524282.1:p.Phe2584Ile
XM_011525981.1:c.7636T>A	XP_011524283.1:p.Phe2546Ile
XM_011525982.1:c.7471T>A	XP_011524284.1:p.Phe2491Ile
XM_011525978.2:c.7768T>A	XP_011524280.1:p.Phe2590Ile
XM_011525979.2:c.7759T>A	XP_011524281.1:p.Phe2587Ile
XM_011525980.2:c.7750T>A	XP_011524282.1:p.Phe2584Ile
XM_011525981.2:c.7636T>A	XP_011524283.1:p.Phe2546Ile
XM_011525982.2:c.7471T>A	XP_011524284.1:p.Phe2491Ile
XM_017025743.1:c.5620T>A	XP_016881232.1:p.Phe1874Ile
XM_017025744.1:c.3310T>A	XP_016881233.1:p.Phe1104Ile
XR_001753199.1:n.8009T>A
NM_000227.5:c.2914T>A	NP_000218.3:p.Phe972Ile
NM_001127717.3:c.7573T>A	NP_001121189.2:p.Phe2525Ile
NM_001127718.3:c.2746T>A	NP_001121190.2:p.Phe916Ile
NM_198129.3:c.7741T>A	NP_937762.2:p.Phe2581Ile
NM_000227.6:c.2914T>A MANE Plus Clinical	NP_000218.3:p.Phe972Ile
NM_001127717.4:c.7573T>A	NP_001121189.2:p.Phe2525Ile
NM_001127718.4:c.2746T>A	NP_001121190.2:p.Phe916Ile
NM_198129.4:c.7741T>A MANE Select	NP_937762.2:p.Phe2581Ile