Canonical Allele Identifier: CA297122864

Gene: LAMA3

Linked Data

• dbSNP Id: rs373385653
• gnomAD v4: 18-23928673-G-A
• MyVariant Identifiers: chr18:g.21508637G>A (hg19) ; chr18:g.23928673G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23928673G>A , CM000680.2:g.23928673G>A	GRCh38
NC_000018.9:g.21508637G>A , CM000680.1:g.21508637G>A	GRCh37
NC_000018.8:g.19762635G>A	NCBI36
NG_007853.2:g.244076G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.3517G>A MANE Plus Clinical	ENSP00000269217.5:p.Asp1173Asn
ENST00000313654.14:c.8344G>A MANE Select	ENSP00000324532.8:p.Asp2782Asn
ENST00000649721.1:c.4939G>A	ENSP00000497885.1:p.Asp1647Asn
ENST00000269217.10:c.3517G>A	ENSP00000269217.5:p.Asp1173Asn
ENST00000313654.13:c.8344G>A	ENSP00000324532.8:p.Asp2782Asn
ENST00000399516.7:c.8176G>A	ENSP00000382432.2:p.Asp2726Asn
ENST00000586751.5:c.3122G>A
ENST00000587184.5:c.3349G>A	ENSP00000466557.1:p.Asp1117Asn
ENST00000588164.2:c.49G>A	ENSP00000467473.2:p.Asp17Asn
ENST00000588770.5:n.2922G>A
NM_000227.4:c.3517G>A	NP_000218.3:p.Asp1173Asn
NM_001127717.2:c.8176G>A	NP_001121189.2:p.Asp2726Asn
NM_001127718.2:c.3349G>A	NP_001121190.2:p.Asp1117Asn
NM_198129.2:c.8344G>A	NP_937762.2:p.Asp2782Asn
XM_011525978.1:c.8371G>A	XP_011524280.1:p.Asp2791Asn
XM_011525979.1:c.8362G>A	XP_011524281.1:p.Asp2788Asn
XM_011525980.1:c.8353G>A	XP_011524282.1:p.Asp2785Asn
XM_011525981.1:c.8239G>A	XP_011524283.1:p.Asp2747Asn
XM_011525982.1:c.8074G>A	XP_011524284.1:p.Asp2692Asn
XM_011525978.2:c.8371G>A	XP_011524280.1:p.Asp2791Asn
XM_011525979.2:c.8362G>A	XP_011524281.1:p.Asp2788Asn
XM_011525980.2:c.8353G>A	XP_011524282.1:p.Asp2785Asn
XM_011525981.2:c.8239G>A	XP_011524283.1:p.Asp2747Asn
XM_011525982.2:c.8074G>A	XP_011524284.1:p.Asp2692Asn
XM_017025743.1:c.6223G>A	XP_016881232.1:p.Asp2075Asn
XM_017025744.1:c.3913G>A	XP_016881233.1:p.Asp1305Asn
XR_001753199.1:n.8612G>A
NM_000227.5:c.3517G>A	NP_000218.3:p.Asp1173Asn
NM_001127717.3:c.8176G>A	NP_001121189.2:p.Asp2726Asn
NM_001127718.3:c.3349G>A	NP_001121190.2:p.Asp1117Asn
NM_198129.3:c.8344G>A	NP_937762.2:p.Asp2782Asn
NM_000227.6:c.3517G>A MANE Plus Clinical	NP_000218.3:p.Asp1173Asn
NM_001127717.4:c.8176G>A	NP_001121189.2:p.Asp2726Asn
NM_001127718.4:c.3349G>A	NP_001121190.2:p.Asp1117Asn
NM_198129.4:c.8344G>A MANE Select	NP_937762.2:p.Asp2782Asn