Canonical Allele Identifier: CA365620118

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129785476G>A (hg19) ; chr6:g.129464331G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129464331G>A , CM000668.2:g.129464331G>A	GRCh38
NC_000006.11:g.129785476G>A , CM000668.1:g.129785476G>A	GRCh37
NC_000006.10:g.129827169G>A	NCBI36
NG_008678.1:g.586191G>A , LRG_409:g.586191G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7034G>A	ENSP00000481744.2:p.Gly2345Glu
ENST00000618192.5:c.7298G>A	ENSP00000480802.2:p.Gly2433Glu
ENST00000684985.1:n.665G>A
ENST00000688150.1:n.373G>A
ENST00000421865.3:c.7034G>A MANE Select	ENSP00000400365.2:p.Gly2345Glu
ENST00000421865.2:c.7034G>A	ENSP00000400365.2:p.Gly2345Glu
ENST00000617695.4:c.7034G>A	ENSP00000481744.1:p.Gly2345Glu
ENST00000618192.4:c.7031G>A	ENSP00000480802.1:p.Gly2344Glu
NM_000426.3:c.7034G>A , LRG_409t1:c.7034G>A	NP_000417.2:p.Gly2345Glu
NM_001079823.1:c.7034G>A	NP_001073291.1:p.Gly2345Glu
XM_005266981.2:c.7298G>A	XP_005267038.1:p.Gly2433Glu
XM_005266982.2:c.7298G>A	XP_005267039.1:p.Gly2433Glu
XM_011535820.1:c.7292G>A	XP_011534122.1:p.Gly2431Glu
XM_005266981.3:c.7298G>A	XP_005267038.1:p.Gly2433Glu
XM_005266982.3:c.7298G>A	XP_005267039.1:p.Gly2433Glu
XM_011535820.2:c.7292G>A	XP_011534122.1:p.Gly2431Glu
XM_017010851.2:c.7304G>A	XP_016866340.1:p.Gly2435Glu
XM_017010852.1:c.5429G>A	XP_016866341.1:p.Gly1810Glu
NM_000426.4:c.7034G>A MANE Select	NP_000417.3:p.Gly2345Glu
NM_001079823.2:c.7034G>A	NP_001073291.2:p.Gly2345Glu