Canonical Allele Identifier: CA451934050

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129802527T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129481382T>G , CM000668.2:g.129481382T>G	GRCh38
NC_000006.11:g.129802527T>G , CM000668.1:g.129802527T>G	GRCh37
NC_000006.10:g.129844220T>G	NCBI36
NG_008678.1:g.603242T>G , LRG_409:g.603242T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000617695.5:c.7680T>G	ENSP00000481744.2:p.Leu2560=
ENST00000618192.5:c.7956T>G	ENSP00000480802.2:p.Leu2652=
ENST00000421865.3:c.7692T>G MANE Select	ENSP00000400365.2:p.Leu2564=
ENST00000421865.2:c.7692T>G	ENSP00000400365.2:p.Leu2564=
ENST00000617695.4:c.7680T>G	ENSP00000481744.1:p.Leu2560=
ENST00000618192.4:c.7689T>G	ENSP00000480802.1:p.Leu2563=
NM_000426.3:c.7692T>G , LRG_409t1:c.7692T>G	NP_000417.2:p.Leu2564=
NM_001079823.1:c.7680T>G	NP_001073291.1:p.Leu2560=
XM_005266981.2:c.7956T>G	XP_005267038.1:p.Leu2652=
XM_005266982.2:c.7944T>G	XP_005267039.1:p.Leu2648=
XM_011535820.1:c.7950T>G	XP_011534122.1:p.Leu2650=
XM_005266981.3:c.7956T>G	XP_005267038.1:p.Leu2652=
XM_005266982.3:c.7944T>G	XP_005267039.1:p.Leu2648=
XM_011535820.2:c.7950T>G	XP_011534122.1:p.Leu2650=
XM_017010851.2:c.7962T>G	XP_016866340.1:p.Leu2654=
XM_017010852.1:c.6087T>G	XP_016866341.1:p.Leu2029=
NM_000426.4:c.7692T>G MANE Select	NP_000417.3:p.Leu2564=
NM_001079823.2:c.7680T>G	NP_001073291.2:p.Leu2560=