Canonical Allele Identifier: CA365612831

Gene: LAMA2

Linked Data

• gnomAD v4: 6-129315552-T-G
• MyVariant Identifiers: chr6:g.129636697T>G (hg19) ; chr6:g.129315552T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129315552T>G , CM000668.2:g.129315552T>G	GRCh38
NC_000006.11:g.129636697T>G , CM000668.1:g.129636697T>G	GRCh37
NC_000006.10:g.129678390T>G	NCBI36
NG_008678.1:g.437412T>G , LRG_409:g.437412T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.3632T>G	ENSP00000481744.2:p.Val1211Gly
ENST00000618192.5:c.3896T>G	ENSP00000480802.2:p.Val1299Gly
ENST00000421865.3:c.3632T>G MANE Select	ENSP00000400365.2:p.Val1211Gly
ENST00000421865.2:c.3632T>G	ENSP00000400365.2:p.Val1211Gly
ENST00000617695.4:c.3632T>G	ENSP00000481744.1:p.Val1211Gly
ENST00000618192.4:c.3632T>G	ENSP00000480802.1:p.Val1211Gly
NM_000426.3:c.3632T>G , LRG_409t1:c.3632T>G	NP_000417.2:p.Val1211Gly
NM_001079823.1:c.3632T>G	NP_001073291.1:p.Val1211Gly
XM_005266981.2:c.3896T>G	XP_005267038.1:p.Val1299Gly
XM_005266982.2:c.3896T>G	XP_005267039.1:p.Val1299Gly
XM_011535820.1:c.3896T>G	XP_011534122.1:p.Val1299Gly
XM_005266981.3:c.3896T>G	XP_005267038.1:p.Val1299Gly
XM_005266982.3:c.3896T>G	XP_005267039.1:p.Val1299Gly
XM_011535820.2:c.3896T>G	XP_011534122.1:p.Val1299Gly
XM_017010851.2:c.3902T>G	XP_016866340.1:p.Val1301Gly
XM_017010852.1:c.2027T>G	XP_016866341.1:p.Val676Gly
XM_017010853.1:c.3896T>G	XP_016866342.1:p.Val1299Gly
NM_000426.4:c.3632T>G MANE Select	NP_000417.3:p.Val1211Gly
NM_001079823.2:c.3632T>G	NP_001073291.2:p.Val1211Gly