Canonical Allele Identifier: CA1663173909

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481434G= , CM000668.2:g.129481434G=	GRCh38
NC_000006.11:g.129802579G= , CM000668.1:g.129802579G=	GRCh37
NC_000006.10:g.129844272G=	NCBI36
NG_008678.1:g.603294G= , LRG_409:g.603294G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7732G=	ENSP00000481744.2:p.Gly2578=
ENST00000618192.5:c.8008G=	ENSP00000480802.2:p.Gly2670=
ENST00000421865.3:c.7744G= MANE Select	ENSP00000400365.2:p.Gly2582=
ENST00000421865.2:c.7744G=	ENSP00000400365.2:p.Gly2582=
ENST00000617695.4:c.7732G=	ENSP00000481744.1:p.Gly2578=
ENST00000618192.4:c.7741G=	ENSP00000480802.1:p.Gly2581=
NM_000426.3:c.7744G= , LRG_409t1:c.7744G=	NP_000417.2:p.Gly2582=
NM_001079823.1:c.7732G=	NP_001073291.1:p.Gly2578=
XM_005266981.2:c.8008G=	XP_005267038.1:p.Gly2670=
XM_005266982.2:c.7996G=	XP_005267039.1:p.Gly2666=
XM_011535820.1:c.8002G=	XP_011534122.1:p.Gly2668=
XM_005266981.3:c.8008G=	XP_005267038.1:p.Gly2670=
XM_005266982.3:c.7996G=	XP_005267039.1:p.Gly2666=
XM_011535820.2:c.8002G=	XP_011534122.1:p.Gly2668=
XM_017010851.2:c.8014G=	XP_016866340.1:p.Gly2672=
XM_017010852.1:c.6139G=	XP_016866341.1:p.Gly2047=
NM_000426.4:c.7744G= MANE Select	NP_000417.3:p.Gly2582=
NM_001079823.2:c.7732G=	NP_001073291.2:p.Gly2578=