Canonical Allele Identifier: CA1663192668

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465243T= , CM000668.2:g.129465243T=	GRCh38
NC_000006.11:g.129786388T= , CM000668.1:g.129786388T=	GRCh37
NC_000006.10:g.129828081T=	NCBI36
NG_008678.1:g.587103T= , LRG_409:g.587103T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7254T=	ENSP00000481744.2:p.Asn2418=
ENST00000618192.5:c.7518T=	ENSP00000480802.2:p.Asn2506=
ENST00000684985.1:n.885T=
ENST00000421865.3:c.7254T= MANE Select	ENSP00000400365.2:p.Asn2418=
ENST00000421865.2:c.7254T=	ENSP00000400365.2:p.Asn2418=
ENST00000617695.4:c.7254T=	ENSP00000481744.1:p.Asn2418=
ENST00000618192.4:c.7251T=	ENSP00000480802.1:p.Asn2417=
NM_000426.3:c.7254T= , LRG_409t1:c.7254T=	NP_000417.2:p.Asn2418=
NM_001079823.1:c.7254T=	NP_001073291.1:p.Asn2418=
XM_005266981.2:c.7518T=	XP_005267038.1:p.Asn2506=
XM_005266982.2:c.7518T=	XP_005267039.1:p.Asn2506=
XM_011535820.1:c.7512T=	XP_011534122.1:p.Asn2504=
XM_005266981.3:c.7518T=	XP_005267038.1:p.Asn2506=
XM_005266982.3:c.7518T=	XP_005267039.1:p.Asn2506=
XM_011535820.2:c.7512T=	XP_011534122.1:p.Asn2504=
XM_017010851.2:c.7524T=	XP_016866340.1:p.Asn2508=
XM_017010852.1:c.5649T=	XP_016866341.1:p.Asn1883=
NM_000426.4:c.7254T= MANE Select	NP_000417.3:p.Asn2418=
NM_001079823.2:c.7254T=	NP_001073291.2:p.Asn2418=