Canonical Allele Identifier: CA244760

Gene: LAMA2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129383131G>A , CM000668.2:g.129383131G>A	GRCh38
NC_000006.11:g.129704276G>A , CM000668.1:g.129704276G>A	GRCh37
NC_000006.10:g.129745969G>A	NCBI36
NG_008678.1:g.504991G>A , LRG_409:g.504991G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.4969G>A	ENSP00000481744.2:p.Val1657Met
ENST00000618192.5:c.5233G>A	ENSP00000480802.2:p.Val1745Met
ENST00000687590.1:n.1389G>A
ENST00000421865.3:c.4969G>A MANE Select	ENSP00000400365.2:p.Val1657Met
ENST00000421865.2:c.4969G>A	ENSP00000400365.2:p.Val1657Met
ENST00000617695.4:c.4969G>A	ENSP00000481744.1:p.Val1657Met
ENST00000618192.4:c.4969G>A	ENSP00000480802.1:p.Val1657Met
NM_000426.3:c.4969G>A , LRG_409t1:c.4969G>A	NP_000417.2:p.Val1657Met
NM_001079823.1:c.4969G>A	NP_001073291.1:p.Val1657Met
XM_005266981.2:c.5233G>A	XP_005267038.1:p.Val1745Met
XM_005266982.2:c.5233G>A	XP_005267039.1:p.Val1745Met
XM_011535820.1:c.5233G>A	XP_011534122.1:p.Val1745Met
XM_005266981.3:c.5233G>A	XP_005267038.1:p.Val1745Met
XM_005266982.3:c.5233G>A	XP_005267039.1:p.Val1745Met
XM_011535820.2:c.5233G>A	XP_011534122.1:p.Val1745Met
XM_017010851.2:c.5239G>A	XP_016866340.1:p.Val1747Met
XM_017010852.1:c.3364G>A	XP_016866341.1:p.Val1122Met
XM_017010853.1:c.5233G>A	XP_016866342.1:p.Val1745Met
NM_000426.4:c.4969G>A MANE Select	NP_000417.3:p.Val1657Met
NM_001079823.2:c.4969G>A	NP_001073291.2:p.Val1657Met