Canonical Allele Identifier: CA1663192594

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129465169A= , CM000668.2:g.129465169A=	GRCh38
NC_000006.11:g.129786314A= , CM000668.1:g.129786314A=	GRCh37
NC_000006.10:g.129828007A=	NCBI36
NG_008678.1:g.587029A= , LRG_409:g.587029A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7180A=	ENSP00000481744.2:p.Thr2394=
ENST00000618192.5:c.7444A=	ENSP00000480802.2:p.Thr2482=
ENST00000684985.1:n.811A=
ENST00000688150.1:n.519A=
ENST00000421865.3:c.7180A= MANE Select	ENSP00000400365.2:p.Thr2394=
ENST00000421865.2:c.7180A=	ENSP00000400365.2:p.Thr2394=
ENST00000617695.4:c.7180A=	ENSP00000481744.1:p.Thr2394=
ENST00000618192.4:c.7177A=	ENSP00000480802.1:p.Thr2393=
NM_000426.3:c.7180A= , LRG_409t1:c.7180A=	NP_000417.2:p.Thr2394=
NM_001079823.1:c.7180A=	NP_001073291.1:p.Thr2394=
XM_005266981.2:c.7444A=	XP_005267038.1:p.Thr2482=
XM_005266982.2:c.7444A=	XP_005267039.1:p.Thr2482=
XM_011535820.1:c.7438A=	XP_011534122.1:p.Thr2480=
XM_005266981.3:c.7444A=	XP_005267038.1:p.Thr2482=
XM_005266982.3:c.7444A=	XP_005267039.1:p.Thr2482=
XM_011535820.2:c.7438A=	XP_011534122.1:p.Thr2480=
XM_017010851.2:c.7450A=	XP_016866340.1:p.Thr2484=
XM_017010852.1:c.5575A=	XP_016866341.1:p.Thr1859=
NM_000426.4:c.7180A= MANE Select	NP_000417.3:p.Thr2394=
NM_001079823.2:c.7180A=	NP_001073291.2:p.Thr2394=