Canonical Allele Identifier: CA402063196

Gene: LAMA3

Linked Data

• MyVariant Identifiers: chr18:g.21508152T>A (hg19) ; chr18:g.23928188T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928188T>A , CM000680.2:g.23928188T>A	GRCh38
NC_000018.9:g.21508152T>A , CM000680.1:g.21508152T>A	GRCh37
NC_000018.8:g.19762150T>A	NCBI36
NG_007853.2:g.243591T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269217.11:c.3416T>A MANE Plus Clinical	ENSP00000269217.5:p.Val1139Asp
ENST00000313654.14:c.8243T>A MANE Select	ENSP00000324532.8:p.Val2748Asp
ENST00000649721.1:c.4838T>A	ENSP00000497885.1:p.Val1613Asp
ENST00000269217.10:c.3416T>A	ENSP00000269217.5:p.Val1139Asp
ENST00000313654.13:c.8243T>A	ENSP00000324532.8:p.Val2748Asp
ENST00000399516.7:c.8075T>A	ENSP00000382432.2:p.Val2692Asp
ENST00000586751.5:c.3021T>A
ENST00000587184.5:c.3248T>A	ENSP00000466557.1:p.Val1083Asp
ENST00000588770.5:n.2821T>A
NM_000227.4:c.3416T>A	NP_000218.3:p.Val1139Asp
NM_001127717.2:c.8075T>A	NP_001121189.2:p.Val2692Asp
NM_001127718.2:c.3248T>A	NP_001121190.2:p.Val1083Asp
NM_198129.2:c.8243T>A	NP_937762.2:p.Val2748Asp
XM_011525978.1:c.8270T>A	XP_011524280.1:p.Val2757Asp
XM_011525979.1:c.8261T>A	XP_011524281.1:p.Val2754Asp
XM_011525980.1:c.8252T>A	XP_011524282.1:p.Val2751Asp
XM_011525981.1:c.8138T>A	XP_011524283.1:p.Val2713Asp
XM_011525982.1:c.7973T>A	XP_011524284.1:p.Val2658Asp
XM_011525978.2:c.8270T>A	XP_011524280.1:p.Val2757Asp
XM_011525979.2:c.8261T>A	XP_011524281.1:p.Val2754Asp
XM_011525980.2:c.8252T>A	XP_011524282.1:p.Val2751Asp
XM_011525981.2:c.8138T>A	XP_011524283.1:p.Val2713Asp
XM_011525982.2:c.7973T>A	XP_011524284.1:p.Val2658Asp
XM_017025743.1:c.6122T>A	XP_016881232.1:p.Val2041Asp
XM_017025744.1:c.3812T>A	XP_016881233.1:p.Val1271Asp
XR_001753199.1:n.8511T>A
NM_000227.5:c.3416T>A	NP_000218.3:p.Val1139Asp
NM_001127717.3:c.8075T>A	NP_001121189.2:p.Val2692Asp
NM_001127718.3:c.3248T>A	NP_001121190.2:p.Val1083Asp
NM_198129.3:c.8243T>A	NP_937762.2:p.Val2748Asp
NM_000227.6:c.3416T>A MANE Plus Clinical	NP_000218.3:p.Val1139Asp
NM_001127717.4:c.8075T>A	NP_001121189.2:p.Val2692Asp
NM_001127718.4:c.3248T>A	NP_001121190.2:p.Val1083Asp
NM_198129.4:c.8243T>A MANE Select	NP_937762.2:p.Val2748Asp