Canonical Allele Identifier: CA1663173893

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481427G= , CM000668.2:g.129481427G=	GRCh38
NC_000006.11:g.129802572G= , CM000668.1:g.129802572G=	GRCh37
NC_000006.10:g.129844265G=	NCBI36
NG_008678.1:g.603287G= , LRG_409:g.603287G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7725G=	ENSP00000481744.2:p.Arg2575=
ENST00000618192.5:c.8001G=	ENSP00000480802.2:p.Arg2667=
ENST00000421865.3:c.7737G= MANE Select	ENSP00000400365.2:p.Arg2579=
ENST00000421865.2:c.7737G=	ENSP00000400365.2:p.Arg2579=
ENST00000617695.4:c.7725G=	ENSP00000481744.1:p.Arg2575=
ENST00000618192.4:c.7734G=	ENSP00000480802.1:p.Arg2578=
NM_000426.3:c.7737G= , LRG_409t1:c.7737G=	NP_000417.2:p.Arg2579=
NM_001079823.1:c.7725G=	NP_001073291.1:p.Arg2575=
XM_005266981.2:c.8001G=	XP_005267038.1:p.Arg2667=
XM_005266982.2:c.7989G=	XP_005267039.1:p.Arg2663=
XM_011535820.1:c.7995G=	XP_011534122.1:p.Arg2665=
XM_005266981.3:c.8001G=	XP_005267038.1:p.Arg2667=
XM_005266982.3:c.7989G=	XP_005267039.1:p.Arg2663=
XM_011535820.2:c.7995G=	XP_011534122.1:p.Arg2665=
XM_017010851.2:c.8007G=	XP_016866340.1:p.Arg2669=
XM_017010852.1:c.6132G=	XP_016866341.1:p.Arg2044=
NM_000426.4:c.7737G= MANE Select	NP_000417.3:p.Arg2579=
NM_001079823.2:c.7725G=	NP_001073291.2:p.Arg2575=