Canonical Allele Identifier: CA402045096

Gene: LAMA3

Linked Data

• ClinVar Variation Id: 552993
• ClinVar RCV Id: RCV000668353 ; RCV001222962
• dbSNP Id: rs1057517023
• gnomAD v4: 18-23876408-G-A
• COSMIC: COSM4580343 ; COSM4580344
• MyVariant Identifiers: chr18:g.21456372G>A (hg19) ; chr18:g.23876408G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.23876408G>A , CM000680.2:g.23876408G>A	GRCh38
NC_000018.9:g.21456372G>A , CM000680.1:g.21456372G>A	GRCh37
NC_000018.8:g.19710370G>A	NCBI36
NG_007853.2:g.191811G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000269217.11:c.285+1G>A MANE Plus Clinical	ENSP00000269217.5:n.285+1G>A
ENST00000313654.14:c.5112+1G>A MANE Select	ENSP00000324532.8:n.5112+1G>A
ENST00000649721.1:c.2004+1G>A	ENSP00000497885.1:n.2004+1G>A
ENST00000269217.10:c.285+1G>A	ENSP00000269217.5:n.285+1G>A
ENST00000313654.13:c.5112+1G>A	ENSP00000324532.8:n.5112+1G>A
ENST00000399516.7:c.5112+1G>A	ENSP00000382432.2:n.5112+1G>A
ENST00000587184.5:c.285+1G>A	ENSP00000466557.1:n.285+1G>A
NM_000227.4:c.285+1G>A	NP_000218.3:n.285+1G>A
NM_001127717.2:c.5112+1G>A	NP_001121189.2:n.5112+1G>A
NM_001127718.2:c.285+1G>A	NP_001121190.2:n.285+1G>A
NM_198129.2:c.5112+1G>A	NP_937762.2:n.5112+1G>A
XM_011525978.1:c.5139+1G>A	XP_011524280.1:n.5139+1G>A
XM_011525979.1:c.5130+1G>A	XP_011524281.1:n.5130+1G>A
XM_011525980.1:c.5121+1G>A	XP_011524282.1:n.5121+1G>A
XM_011525981.1:c.5007+1G>A	XP_011524283.1:n.5007+1G>A
XM_011525982.1:c.5139+1G>A	XP_011524284.1:n.5139+1G>A
XM_011525978.2:c.5139+1G>A	XP_011524280.1:n.5139+1G>A
XM_011525979.2:c.5130+1G>A	XP_011524281.1:n.5130+1G>A
XM_011525980.2:c.5121+1G>A	XP_011524282.1:n.5121+1G>A
XM_011525981.2:c.5007+1G>A	XP_011524283.1:n.5007+1G>A
XM_011525982.2:c.5139+1G>A	XP_011524284.1:n.5139+1G>A
XM_017025743.1:c.2991+1G>A	XP_016881232.1:n.2991+1G>A
XM_017025744.1:c.681+1G>A	XP_016881233.1:n.681+1G>A
XR_001753199.1:n.5380+1G>A
NM_000227.5:c.285+1G>A	NP_000218.3:n.285+1G>A
NM_001127717.3:c.5112+1G>A	NP_001121189.2:n.5112+1G>A
NM_001127718.3:c.285+1G>A	NP_001121190.2:n.285+1G>A
NM_198129.3:c.5112+1G>A	NP_937762.2:n.5112+1G>A
NM_000227.6:c.285+1G>A MANE Plus Clinical	NP_000218.3:n.285+1G>A
NM_001127717.4:c.5112+1G>A	NP_001121189.2:n.5112+1G>A
NM_001127718.4:c.285+1G>A	NP_001121190.2:n.285+1G>A
NM_198129.4:c.5112+1G>A MANE Select	NP_937762.2:n.5112+1G>A