Canonical Allele Identifier: CA1663173796

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481381T= , CM000668.2:g.129481381T=	GRCh38
NC_000006.11:g.129802526T= , CM000668.1:g.129802526T=	GRCh37
NC_000006.10:g.129844219T=	NCBI36
NG_008678.1:g.603241T= , LRG_409:g.603241T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7679T=	ENSP00000481744.2:p.Leu2560=
ENST00000618192.5:c.7955T=	ENSP00000480802.2:p.Leu2652=
ENST00000421865.3:c.7691T= MANE Select	ENSP00000400365.2:p.Leu2564=
ENST00000421865.2:c.7691T=	ENSP00000400365.2:p.Leu2564=
ENST00000617695.4:c.7679T=	ENSP00000481744.1:p.Leu2560=
ENST00000618192.4:c.7688T=	ENSP00000480802.1:p.Leu2563=
NM_000426.3:c.7691T= , LRG_409t1:c.7691T=	NP_000417.2:p.Leu2564=
NM_001079823.1:c.7679T=	NP_001073291.1:p.Leu2560=
XM_005266981.2:c.7955T=	XP_005267038.1:p.Leu2652=
XM_005266982.2:c.7943T=	XP_005267039.1:p.Leu2648=
XM_011535820.1:c.7949T=	XP_011534122.1:p.Leu2650=
XM_005266981.3:c.7955T=	XP_005267038.1:p.Leu2652=
XM_005266982.3:c.7943T=	XP_005267039.1:p.Leu2648=
XM_011535820.2:c.7949T=	XP_011534122.1:p.Leu2650=
XM_017010851.2:c.7961T=	XP_016866340.1:p.Leu2654=
XM_017010852.1:c.6086T=	XP_016866341.1:p.Leu2029=
NM_000426.4:c.7691T= MANE Select	NP_000417.3:p.Leu2564=
NM_001079823.2:c.7679T=	NP_001073291.2:p.Leu2560=