Canonical Allele Identifier: CA451925859

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129785495C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129464350C>A , CM000668.2:g.129464350C>A	GRCh38
NC_000006.11:g.129785495C>A , CM000668.1:g.129785495C>A	GRCh37
NC_000006.10:g.129827188C>A	NCBI36
NG_008678.1:g.586210C>A , LRG_409:g.586210C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000617695.5:c.7053C>A	ENSP00000481744.2:p.Val2351=
ENST00000618192.5:c.7317C>A	ENSP00000480802.2:p.Val2439=
ENST00000684985.1:n.684C>A
ENST00000688150.1:n.392C>A
ENST00000421865.3:c.7053C>A MANE Select	ENSP00000400365.2:p.Val2351=
ENST00000421865.2:c.7053C>A	ENSP00000400365.2:p.Val2351=
ENST00000617695.4:c.7053C>A	ENSP00000481744.1:p.Val2351=
ENST00000618192.4:c.7050C>A	ENSP00000480802.1:p.Val2350=
NM_000426.3:c.7053C>A , LRG_409t1:c.7053C>A	NP_000417.2:p.Val2351=
NM_001079823.1:c.7053C>A	NP_001073291.1:p.Val2351=
XM_005266981.2:c.7317C>A	XP_005267038.1:p.Val2439=
XM_005266982.2:c.7317C>A	XP_005267039.1:p.Val2439=
XM_011535820.1:c.7311C>A	XP_011534122.1:p.Val2437=
XM_005266981.3:c.7317C>A	XP_005267038.1:p.Val2439=
XM_005266982.3:c.7317C>A	XP_005267039.1:p.Val2439=
XM_011535820.2:c.7311C>A	XP_011534122.1:p.Val2437=
XM_017010851.2:c.7323C>A	XP_016866340.1:p.Val2441=
XM_017010852.1:c.5448C>A	XP_016866341.1:p.Val1816=
NM_000426.4:c.7053C>A MANE Select	NP_000417.3:p.Val2351=
NM_001079823.2:c.7053C>A	NP_001073291.2:p.Val2351=