Canonical Allele Identifier: CA1663192714

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465286C= , CM000668.2:g.129465286C=	GRCh38
NC_000006.11:g.129786431C= , CM000668.1:g.129786431C=	GRCh37
NC_000006.10:g.129828124C=	NCBI36
NG_008678.1:g.587146C= , LRG_409:g.587146C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7297C=	ENSP00000481744.2:p.Gln2433=
ENST00000618192.5:c.7561C=	ENSP00000480802.2:p.Gln2521=
ENST00000684985.1:n.928C=
ENST00000421865.3:c.7297C= MANE Select	ENSP00000400365.2:p.Gln2433=
ENST00000421865.2:c.7297C=	ENSP00000400365.2:p.Gln2433=
ENST00000617695.4:c.7297C=	ENSP00000481744.1:p.Gln2433=
ENST00000618192.4:c.7294C=	ENSP00000480802.1:p.Gln2432=
NM_000426.3:c.7297C= , LRG_409t1:c.7297C=	NP_000417.2:p.Gln2433=
NM_001079823.1:c.7297C=	NP_001073291.1:p.Gln2433=
XM_005266981.2:c.7561C=	XP_005267038.1:p.Gln2521=
XM_005266982.2:c.7561C=	XP_005267039.1:p.Gln2521=
XM_011535820.1:c.7555C=	XP_011534122.1:p.Gln2519=
XM_005266981.3:c.7561C=	XP_005267038.1:p.Gln2521=
XM_005266982.3:c.7561C=	XP_005267039.1:p.Gln2521=
XM_011535820.2:c.7555C=	XP_011534122.1:p.Gln2519=
XM_017010851.2:c.7567C=	XP_016866340.1:p.Gln2523=
XM_017010852.1:c.5692C=	XP_016866341.1:p.Gln1898=
NM_000426.4:c.7297C= MANE Select	NP_000417.3:p.Gln2433=
NM_001079823.2:c.7297C=	NP_001073291.2:p.Gln2433=