Canonical Allele Identifier: CA1663157859

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129505232T= , CM000668.2:g.129505232T=	GRCh38
NC_000006.11:g.129826377T= , CM000668.1:g.129826377T=	GRCh37
NC_000006.10:g.129868070T=	NCBI36
NG_008678.1:g.627092T= , LRG_409:g.627092T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.645T=	ENSP00000510626.1:p.Ile215=
ENST00000498257.6:c.645T=	ENSP00000510533.1:p.Ile215=
ENST00000617695.5:c.8568T=	ENSP00000481744.2:p.Ile2856=
ENST00000618192.5:c.8844T=	ENSP00000480802.2:p.Ile2948=
ENST00000688198.1:n.1558T=
ENST00000688799.1:c.645T=	ENSP00000508458.1:p.Ile215=
ENST00000690858.1:n.1574T=
ENST00000693461.1:n.917T=
ENST00000421865.3:c.8580T= MANE Select	ENSP00000400365.2:p.Ile2860=
ENST00000421865.2:c.8580T=	ENSP00000400365.2:p.Ile2860=
ENST00000617695.4:c.8568T=	ENSP00000481744.1:p.Ile2856=
ENST00000618192.4:c.8577T=	ENSP00000480802.1:p.Ile2859=
NM_000426.3:c.8580T= , LRG_409t1:c.8580T=	NP_000417.2:p.Ile2860=
NM_001079823.1:c.8568T=	NP_001073291.1:p.Ile2856=
XM_005266981.2:c.8844T=	XP_005267038.1:p.Ile2948=
XM_005266982.2:c.8832T=	XP_005267039.1:p.Ile2944=
XM_011535820.1:c.8838T=	XP_011534122.1:p.Ile2946=
XR_942984.1:n.1461-2441A=
XR_942985.1:n.1325-2441A=
XM_005266981.3:c.8844T=	XP_005267038.1:p.Ile2948=
XM_005266982.3:c.8832T=	XP_005267039.1:p.Ile2944=
XM_011535820.2:c.8838T=	XP_011534122.1:p.Ile2946=
XM_017010851.2:c.8850T=	XP_016866340.1:p.Ile2950=
XM_017010852.1:c.6975T=	XP_016866341.1:p.Ile2325=
XR_001743859.1:n.3901-2441A=
XR_001743860.1:n.1180-2441A=
XR_001743861.1:n.1347-2441A=
XR_001743863.1:n.883-2441A=
XR_002956395.1:n.9132-2441A=
XR_002956396.1:n.3127-2441A=
NM_000426.4:c.8580T= MANE Select	NP_000417.3:p.Ile2860=
NM_001079823.2:c.8568T=	NP_001073291.2:p.Ile2856=