Canonical Allele Identifier: CA3993565

Gene: LAMA2

Linked Data

• ClinVar Variation Id: 449238
• ClinVar RCV Id: RCV000520057 ; RCV000714624 ; RCV000714625 ; RCV001821455
• dbSNP Id: rs375640462
• ExAC: 6:129670477 G / A
• gnomAD v2: 6-129670477-G-A
• gnomAD v3: 6-129349332-G-A
• gnomAD v4: 6-129349332-G-A
• MyVariant Identifiers: chr6:g.129670477G>A (hg19) ; chr6:g.129349332G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129349332G>A , CM000668.2:g.129349332G>A	GRCh38
NC_000006.11:g.129670477G>A , CM000668.1:g.129670477G>A	GRCh37
NC_000006.10:g.129712170G>A	NCBI36
NG_008678.1:g.471192G>A , LRG_409:g.471192G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.4471G>A	ENSP00000481744.2:p.Asp1491Asn
ENST00000618192.5:c.4735G>A	ENSP00000480802.2:p.Asp1579Asn
ENST00000692206.1:n.120G>A
ENST00000421865.3:c.4471G>A MANE Select	ENSP00000400365.2:p.Asp1491Asn
ENST00000421865.2:c.4471G>A	ENSP00000400365.2:p.Asp1491Asn
ENST00000617695.4:c.4471G>A	ENSP00000481744.1:p.Asp1491Asn
ENST00000618192.4:c.4471G>A	ENSP00000480802.1:p.Asp1491Asn
NM_000426.3:c.4471G>A , LRG_409t1:c.4471G>A	NP_000417.2:p.Asp1491Asn
NM_001079823.1:c.4471G>A	NP_001073291.1:p.Asp1491Asn
XM_005266981.2:c.4735G>A	XP_005267038.1:p.Asp1579Asn
XM_005266982.2:c.4735G>A	XP_005267039.1:p.Asp1579Asn
XM_011535820.1:c.4735G>A	XP_011534122.1:p.Asp1579Asn
XM_005266981.3:c.4735G>A	XP_005267038.1:p.Asp1579Asn
XM_005266982.3:c.4735G>A	XP_005267039.1:p.Asp1579Asn
XM_011535820.2:c.4735G>A	XP_011534122.1:p.Asp1579Asn
XM_017010851.2:c.4741G>A	XP_016866340.1:p.Asp1581Asn
XM_017010852.1:c.2866G>A	XP_016866341.1:p.Asp956Asn
XM_017010853.1:c.4735G>A	XP_016866342.1:p.Asp1579Asn
NM_000426.4:c.4471G>A MANE Select	NP_000417.3:p.Asp1491Asn
NM_001079823.2:c.4471G>A	NP_001073291.2:p.Asp1491Asn