Canonical Allele Identifier: CA365617459

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129349342-G-A
• MyVariant Identifiers: chr6:g.129670487G>A (hg19) ; chr6:g.129349342G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129349342G>A , CM000668.2:g.129349342G>A	GRCh38
NC_000006.11:g.129670487G>A , CM000668.1:g.129670487G>A	GRCh37
NC_000006.10:g.129712180G>A	NCBI36
NG_008678.1:g.471202G>A , LRG_409:g.471202G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.4481G>A	ENSP00000481744.2:p.Cys1494Tyr
ENST00000618192.5:c.4745G>A	ENSP00000480802.2:p.Cys1582Tyr
ENST00000692206.1:n.130G>A
ENST00000693425.1:n.7G>A
ENST00000421865.3:c.4481G>A MANE Select	ENSP00000400365.2:p.Cys1494Tyr
ENST00000421865.2:c.4481G>A	ENSP00000400365.2:p.Cys1494Tyr
ENST00000617695.4:c.4481G>A	ENSP00000481744.1:p.Cys1494Tyr
ENST00000618192.4:c.4481G>A	ENSP00000480802.1:p.Cys1494Tyr
NM_000426.3:c.4481G>A , LRG_409t1:c.4481G>A	NP_000417.2:p.Cys1494Tyr
NM_001079823.1:c.4481G>A	NP_001073291.1:p.Cys1494Tyr
XM_005266981.2:c.4745G>A	XP_005267038.1:p.Cys1582Tyr
XM_005266982.2:c.4745G>A	XP_005267039.1:p.Cys1582Tyr
XM_011535820.1:c.4745G>A	XP_011534122.1:p.Cys1582Tyr
XM_005266981.3:c.4745G>A	XP_005267038.1:p.Cys1582Tyr
XM_005266982.3:c.4745G>A	XP_005267039.1:p.Cys1582Tyr
XM_011535820.2:c.4745G>A	XP_011534122.1:p.Cys1582Tyr
XM_017010851.2:c.4751G>A	XP_016866340.1:p.Cys1584Tyr
XM_017010852.1:c.2876G>A	XP_016866341.1:p.Cys959Tyr
XM_017010853.1:c.4745G>A	XP_016866342.1:p.Cys1582Tyr
NM_000426.4:c.4481G>A MANE Select	NP_000417.3:p.Cys1494Tyr
NM_001079823.2:c.4481G>A	NP_001073291.2:p.Cys1494Tyr