Canonical Allele Identifier: CA2842650071

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129250218_129250219del , CM000668.2:g.129250218_129250219del	GRCh38
NC_000006.11:g.129571363_129571364del , CM000668.1:g.129571363_129571364del	GRCh37
NC_000006.10:g.129613056_129613057del	NCBI36
NG_008678.1:g.372078_372079del , LRG_409:g.372078_372079del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.1884+5_1884+6del	ENSP00000481744.2:n.1884+5_1884+6del
ENST00000618192.5:c.1884+5_1884+6del	ENSP00000480802.2:n.1884+5_1884+6del
ENST00000421865.3:c.1884+5_1884+6del MANE Select	ENSP00000400365.2:n.1884+5_1884+6del
ENST00000421865.2:c.1884+5_1884+6del	ENSP00000400365.2:n.1884+5_1884+6del
ENST00000617695.4:c.1884+5_1884+6del	ENSP00000481744.1:n.1884+5_1884+6del
ENST00000618192.4:c.1884+5_1884+6del	ENSP00000480802.1:n.1884+5_1884+6del
NM_000426.3:c.1884+5_1884+6del , LRG_409t1:c.1884+5_1884+6del	NP_000417.2:n.1884+5_1884+6del
NM_001079823.1:c.1884+5_1884+6del	NP_001073291.1:n.1884+5_1884+6del
XM_005266981.2:c.1884+5_1884+6del	XP_005267038.1:n.1884+5_1884+6del
XM_005266982.2:c.1884+5_1884+6del	XP_005267039.1:n.1884+5_1884+6del
XM_011535820.1:c.1884+5_1884+6del	XP_011534122.1:n.1884+5_1884+6del
XM_005266981.3:c.1884+5_1884+6del	XP_005267038.1:n.1884+5_1884+6del
XM_005266982.3:c.1884+5_1884+6del	XP_005267039.1:n.1884+5_1884+6del
XM_011535820.2:c.1884+5_1884+6del	XP_011534122.1:n.1884+5_1884+6del
XM_017010851.2:c.1890+5_1890+6del	XP_016866340.1:n.1890+5_1890+6del
XM_017010852.1:c.15+5_15+6del	XP_016866341.1:n.15+5_15+6del
XM_017010853.1:c.1884+5_1884+6del	XP_016866342.1:n.1884+5_1884+6del
NM_000426.4:c.1884+5_1884+6del MANE Select	NP_000417.3:n.1884+5_1884+6del
NM_001079823.2:c.1884+5_1884+6del	NP_001073291.2:n.1884+5_1884+6del