Canonical Allele Identifier: CA1663192625

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465196G= , CM000668.2:g.129465196G=	GRCh38
NC_000006.11:g.129786341G= , CM000668.1:g.129786341G=	GRCh37
NC_000006.10:g.129828034G=	NCBI36
NG_008678.1:g.587056G= , LRG_409:g.587056G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7207G=	ENSP00000481744.2:p.Asp2403=
ENST00000618192.5:c.7471G=	ENSP00000480802.2:p.Asp2491=
ENST00000684985.1:n.838G=
ENST00000688150.1:n.546G=
ENST00000421865.3:c.7207G= MANE Select	ENSP00000400365.2:p.Asp2403=
ENST00000421865.2:c.7207G=	ENSP00000400365.2:p.Asp2403=
ENST00000617695.4:c.7207G=	ENSP00000481744.1:p.Asp2403=
ENST00000618192.4:c.7204G=	ENSP00000480802.1:p.Asp2402=
NM_000426.3:c.7207G= , LRG_409t1:c.7207G=	NP_000417.2:p.Asp2403=
NM_001079823.1:c.7207G=	NP_001073291.1:p.Asp2403=
XM_005266981.2:c.7471G=	XP_005267038.1:p.Asp2491=
XM_005266982.2:c.7471G=	XP_005267039.1:p.Asp2491=
XM_011535820.1:c.7465G=	XP_011534122.1:p.Asp2489=
XM_005266981.3:c.7471G=	XP_005267038.1:p.Asp2491=
XM_005266982.3:c.7471G=	XP_005267039.1:p.Asp2491=
XM_011535820.2:c.7465G=	XP_011534122.1:p.Asp2489=
XM_017010851.2:c.7477G=	XP_016866340.1:p.Asp2493=
XM_017010852.1:c.5602G=	XP_016866341.1:p.Asp1868=
NM_000426.4:c.7207G= MANE Select	NP_000417.3:p.Asp2403=
NM_001079823.2:c.7207G=	NP_001073291.2:p.Asp2403=