Canonical Allele Identifier: CA1094385267

Gene: LAMA2

Linked Data

• dbSNP Id: rs1776724247
• gnomAD v3: 6-129349242-A-G
• gnomAD v4: 6-129349242-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129349242A>G , CM000668.2:g.129349242A>G	GRCh38
NC_000006.11:g.129670387A>G , CM000668.1:g.129670387A>G	GRCh37
NC_000006.10:g.129712080A>G	NCBI36
NG_008678.1:g.471102A>G , LRG_409:g.471102A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.4437-56A>G	ENSP00000481744.2:n.4437-56A>G
ENST00000618192.5:c.4701-56A>G	ENSP00000480802.2:n.4701-56A>G
ENST00000692206.1:n.86-56A>G
ENST00000421865.3:c.4437-56A>G MANE Select	ENSP00000400365.2:n.4437-56A>G
ENST00000421865.2:c.4437-56A>G	ENSP00000400365.2:n.4437-56A>G
ENST00000617695.4:c.4437-56A>G	ENSP00000481744.1:n.4437-56A>G
ENST00000618192.4:c.4437-56A>G	ENSP00000480802.1:n.4437-56A>G
NM_000426.3:c.4437-56A>G , LRG_409t1:c.4437-56A>G	NP_000417.2:n.4437-56A>G
NM_001079823.1:c.4437-56A>G	NP_001073291.1:n.4437-56A>G
XM_005266981.2:c.4701-56A>G	XP_005267038.1:n.4701-56A>G
XM_005266982.2:c.4701-56A>G	XP_005267039.1:n.4701-56A>G
XM_011535820.1:c.4701-56A>G	XP_011534122.1:n.4701-56A>G
XM_005266981.3:c.4701-56A>G	XP_005267038.1:n.4701-56A>G
XM_005266982.3:c.4701-56A>G	XP_005267039.1:n.4701-56A>G
XM_011535820.2:c.4701-56A>G	XP_011534122.1:n.4701-56A>G
XM_017010851.2:c.4707-56A>G	XP_016866340.1:n.4707-56A>G
XM_017010852.1:c.2832-56A>G	XP_016866341.1:n.2832-56A>G
XM_017010853.1:c.4701-56A>G	XP_016866342.1:n.4701-56A>G
NM_000426.4:c.4437-56A>G MANE Select	NP_000417.3:n.4437-56A>G
NM_001079823.2:c.4437-56A>G	NP_001073291.2:n.4437-56A>G