Canonical Allele Identifier: CA1663173907

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481432C= , CM000668.2:g.129481432C=	GRCh38
NC_000006.11:g.129802577C= , CM000668.1:g.129802577C=	GRCh37
NC_000006.10:g.129844270C=	NCBI36
NG_008678.1:g.603292C= , LRG_409:g.603292C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7730C=	ENSP00000481744.2:p.Thr2577=
ENST00000618192.5:c.8006C=	ENSP00000480802.2:p.Thr2669=
ENST00000421865.3:c.7742C= MANE Select	ENSP00000400365.2:p.Thr2581=
ENST00000421865.2:c.7742C=	ENSP00000400365.2:p.Thr2581=
ENST00000617695.4:c.7730C=	ENSP00000481744.1:p.Thr2577=
ENST00000618192.4:c.7739C=	ENSP00000480802.1:p.Thr2580=
NM_000426.3:c.7742C= , LRG_409t1:c.7742C=	NP_000417.2:p.Thr2581=
NM_001079823.1:c.7730C=	NP_001073291.1:p.Thr2577=
XM_005266981.2:c.8006C=	XP_005267038.1:p.Thr2669=
XM_005266982.2:c.7994C=	XP_005267039.1:p.Thr2665=
XM_011535820.1:c.8000C=	XP_011534122.1:p.Thr2667=
XM_005266981.3:c.8006C=	XP_005267038.1:p.Thr2669=
XM_005266982.3:c.7994C=	XP_005267039.1:p.Thr2665=
XM_011535820.2:c.8000C=	XP_011534122.1:p.Thr2667=
XM_017010851.2:c.8012C=	XP_016866340.1:p.Thr2671=
XM_017010852.1:c.6137C=	XP_016866341.1:p.Thr2046=
NM_000426.4:c.7742C= MANE Select	NP_000417.3:p.Thr2581=
NM_001079823.2:c.7730C=	NP_001073291.2:p.Thr2577=