Canonical Allele Identifier: CA451934055

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802533A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481388A>T , CM000668.2:g.129481388A>T	GRCh38
NC_000006.11:g.129802533A>T , CM000668.1:g.129802533A>T	GRCh37
NC_000006.10:g.129844226A>T	NCBI36
NG_008678.1:g.603248A>T , LRG_409:g.603248A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7686A>T	ENSP00000481744.2:p.Gly2562=
ENST00000618192.5:c.7962A>T	ENSP00000480802.2:p.Gly2654=
ENST00000421865.3:c.7698A>T MANE Select	ENSP00000400365.2:p.Gly2566=
ENST00000421865.2:c.7698A>T	ENSP00000400365.2:p.Gly2566=
ENST00000617695.4:c.7686A>T	ENSP00000481744.1:p.Gly2562=
ENST00000618192.4:c.7695A>T	ENSP00000480802.1:p.Gly2565=
NM_000426.3:c.7698A>T , LRG_409t1:c.7698A>T	NP_000417.2:p.Gly2566=
NM_001079823.1:c.7686A>T	NP_001073291.1:p.Gly2562=
XM_005266981.2:c.7962A>T	XP_005267038.1:p.Gly2654=
XM_005266982.2:c.7950A>T	XP_005267039.1:p.Gly2650=
XM_011535820.1:c.7956A>T	XP_011534122.1:p.Gly2652=
XM_005266981.3:c.7962A>T	XP_005267038.1:p.Gly2654=
XM_005266982.3:c.7950A>T	XP_005267039.1:p.Gly2650=
XM_011535820.2:c.7956A>T	XP_011534122.1:p.Gly2652=
XM_017010851.2:c.7968A>T	XP_016866340.1:p.Gly2656=
XM_017010852.1:c.6093A>T	XP_016866341.1:p.Gly2031=
NM_000426.4:c.7698A>T MANE Select	NP_000417.3:p.Gly2566=
NM_001079823.2:c.7686A>T	NP_001073291.2:p.Gly2562=