Canonical Allele Identifier: CA2838401856

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129349213C>A , CM000668.2:g.129349213C>A	GRCh38
NC_000006.11:g.129670358C>A , CM000668.1:g.129670358C>A	GRCh37
NC_000006.10:g.129712051C>A	NCBI36
NG_008678.1:g.471073C>A , LRG_409:g.471073C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.4437-85C>A	ENSP00000481744.2:n.4437-85C>A
ENST00000618192.5:c.4701-85C>A	ENSP00000480802.2:n.4701-85C>A
ENST00000692206.1:n.86-85C>A
ENST00000421865.3:c.4437-85C>A MANE Select	ENSP00000400365.2:n.4437-85C>A
ENST00000421865.2:c.4437-85C>A	ENSP00000400365.2:n.4437-85C>A
ENST00000617695.4:c.4437-85C>A	ENSP00000481744.1:n.4437-85C>A
ENST00000618192.4:c.4437-85C>A	ENSP00000480802.1:n.4437-85C>A
NM_000426.3:c.4437-85C>A , LRG_409t1:c.4437-85C>A	NP_000417.2:n.4437-85C>A
NM_001079823.1:c.4437-85C>A	NP_001073291.1:n.4437-85C>A
XM_005266981.2:c.4701-85C>A	XP_005267038.1:n.4701-85C>A
XM_005266982.2:c.4701-85C>A	XP_005267039.1:n.4701-85C>A
XM_011535820.1:c.4701-85C>A	XP_011534122.1:n.4701-85C>A
XM_005266981.3:c.4701-85C>A	XP_005267038.1:n.4701-85C>A
XM_005266982.3:c.4701-85C>A	XP_005267039.1:n.4701-85C>A
XM_011535820.2:c.4701-85C>A	XP_011534122.1:n.4701-85C>A
XM_017010851.2:c.4707-85C>A	XP_016866340.1:n.4707-85C>A
XM_017010852.1:c.2832-85C>A	XP_016866341.1:n.2832-85C>A
XM_017010853.1:c.4701-85C>A	XP_016866342.1:n.4701-85C>A
NM_000426.4:c.4437-85C>A MANE Select	NP_000417.3:n.4437-85C>A
NM_001079823.2:c.4437-85C>A	NP_001073291.2:n.4437-85C>A