Canonical Allele Identifier: CA2580074881

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.128883303dup , CM000668.2:g.128883303dup	GRCh38
NC_000006.11:g.129204448dup , CM000668.1:g.129204448dup	GRCh37
NC_000006.10:g.129246141dup	NCBI36
NG_008678.1:g.5163dup , LRG_409:g.5163dup

Transcript Alleles

HGVS	Amino-acid Change
NM_000426.4:c.58dup MANE Select	NP_000417.3:p.Val20GlyfsTer30
ENST00000421865.3:c.58dup MANE Select	ENSP00000400365.2:p.Val20GlyfsTer30
NM_000426.3:c.58dup , LRG_409t1:c.58dup	NP_000417.2:p.Val20GlyfsTer30
NM_001079823.1:c.58dup	NP_001073291.1:p.Val20GlyfsTer30
NM_001079823.2:c.58dup	NP_001073291.2:p.Val20GlyfsTer30
ENST00000421865.2:c.58dup	ENSP00000400365.2:p.Val20GlyfsTer30
ENST00000617695.4:c.58dup	ENSP00000481744.1:p.Val20GlyfsTer30
ENST00000617695.5:c.58dup	ENSP00000481744.2:p.Val20GlyfsTer30
ENST00000618192.4:c.58dup	ENSP00000480802.1:p.Val20GlyfsTer30
ENST00000618192.5:c.58dup	ENSP00000480802.2:p.Val20GlyfsTer30
ENST00000686577.1:n.124dup
ENST00000686599.1:n.163dup
XM_005266981.2:c.58dup	XP_005267038.1:p.Val20GlyfsTer30
XM_005266981.3:c.58dup	XP_005267038.1:p.Val20GlyfsTer30
XM_005266982.2:c.58dup	XP_005267039.1:p.Val20GlyfsTer30
XM_005266982.3:c.58dup	XP_005267039.1:p.Val20GlyfsTer30
XM_011535820.1:c.58dup	XP_011534122.1:p.Val20GlyfsTer30
XM_011535820.2:c.58dup	XP_011534122.1:p.Val20GlyfsTer30
XM_017010853.1:c.58dup	XP_016866342.1:p.Val20GlyfsTer30