Canonical Allele Identifier: CA1663120352

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129353285C= , CM000668.2:g.129353285C=	GRCh38
NC_000006.11:g.129674430C= , CM000668.1:g.129674430C=	GRCh37
NC_000006.10:g.129716123C=	NCBI36
NG_008678.1:g.475145C= , LRG_409:g.475145C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.4645C=	ENSP00000481744.2:p.Arg1549=
ENST00000618192.5:c.4909C=	ENSP00000480802.2:p.Arg1637=
ENST00000692206.1:n.294C=
ENST00000693425.1:n.171C=
ENST00000421865.3:c.4645C= MANE Select	ENSP00000400365.2:p.Arg1549=
ENST00000421865.2:c.4645C=	ENSP00000400365.2:p.Arg1549=
ENST00000617695.4:c.4645C=	ENSP00000481744.1:p.Arg1549=
ENST00000618192.4:c.4645C=	ENSP00000480802.1:p.Arg1549=
NM_000426.3:c.4645C= , LRG_409t1:c.4645C=	NP_000417.2:p.Arg1549=
NM_001079823.1:c.4645C=	NP_001073291.1:p.Arg1549=
XM_005266981.2:c.4909C=	XP_005267038.1:p.Arg1637=
XM_005266982.2:c.4909C=	XP_005267039.1:p.Arg1637=
XM_011535820.1:c.4909C=	XP_011534122.1:p.Arg1637=
XM_005266981.3:c.4909C=	XP_005267038.1:p.Arg1637=
XM_005266982.3:c.4909C=	XP_005267039.1:p.Arg1637=
XM_011535820.2:c.4909C=	XP_011534122.1:p.Arg1637=
XM_017010851.2:c.4915C=	XP_016866340.1:p.Arg1639=
XM_017010852.1:c.3040C=	XP_016866341.1:p.Arg1014=
XM_017010853.1:c.4909C=	XP_016866342.1:p.Arg1637=
NM_000426.4:c.4645C= MANE Select	NP_000417.3:p.Arg1549=
NM_001079823.2:c.4645C=	NP_001073291.2:p.Arg1549=