Canonical Allele Identifier: CA1663115120

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129349334C= , CM000668.2:g.129349334C=	GRCh38
NC_000006.11:g.129670479C= , CM000668.1:g.129670479C=	GRCh37
NC_000006.10:g.129712172C=	NCBI36
NG_008678.1:g.471194C= , LRG_409:g.471194C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.4473C=	ENSP00000481744.2:p.Asp1491=
ENST00000618192.5:c.4737C=	ENSP00000480802.2:p.Asp1579=
ENST00000692206.1:n.122C=
ENST00000421865.3:c.4473C= MANE Select	ENSP00000400365.2:p.Asp1491=
ENST00000421865.2:c.4473C=	ENSP00000400365.2:p.Asp1491=
ENST00000617695.4:c.4473C=	ENSP00000481744.1:p.Asp1491=
ENST00000618192.4:c.4473C=	ENSP00000480802.1:p.Asp1491=
NM_000426.3:c.4473C= , LRG_409t1:c.4473C=	NP_000417.2:p.Asp1491=
NM_001079823.1:c.4473C=	NP_001073291.1:p.Asp1491=
XM_005266981.2:c.4737C=	XP_005267038.1:p.Asp1579=
XM_005266982.2:c.4737C=	XP_005267039.1:p.Asp1579=
XM_011535820.1:c.4737C=	XP_011534122.1:p.Asp1579=
XM_005266981.3:c.4737C=	XP_005267038.1:p.Asp1579=
XM_005266982.3:c.4737C=	XP_005267039.1:p.Asp1579=
XM_011535820.2:c.4737C=	XP_011534122.1:p.Asp1579=
XM_017010851.2:c.4743C=	XP_016866340.1:p.Asp1581=
XM_017010852.1:c.2868C=	XP_016866341.1:p.Asp956=
XM_017010853.1:c.4737C=	XP_016866342.1:p.Asp1579=
NM_000426.4:c.4473C= MANE Select	NP_000417.3:p.Asp1491=
NM_001079823.2:c.4473C=	NP_001073291.2:p.Asp1491=