Canonical Allele Identifier: CA451935754

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129826398C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129505253C>G , CM000668.2:g.129505253C>G	GRCh38
NC_000006.11:g.129826398C>G , CM000668.1:g.129826398C>G	GRCh37
NC_000006.10:g.129868091C>G	NCBI36
NG_008678.1:g.627113C>G , LRG_409:g.627113C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.666C>G	ENSP00000510626.1:p.Ser222=
ENST00000498257.6:c.666C>G	ENSP00000510533.1:p.Ser222=
ENST00000617695.5:c.8589C>G	ENSP00000481744.2:p.Ser2863=
ENST00000618192.5:c.8865C>G	ENSP00000480802.2:p.Ser2955=
ENST00000688198.1:n.1579C>G
ENST00000688799.1:c.666C>G	ENSP00000508458.1:p.Ser222=
ENST00000690858.1:n.1595C>G
ENST00000693461.1:n.938C>G
ENST00000421865.3:c.8601C>G MANE Select	ENSP00000400365.2:p.Ser2867=
ENST00000421865.2:c.8601C>G	ENSP00000400365.2:p.Ser2867=
ENST00000617695.4:c.8589C>G	ENSP00000481744.1:p.Ser2863=
ENST00000618192.4:c.8598C>G	ENSP00000480802.1:p.Ser2866=
NM_000426.3:c.8601C>G , LRG_409t1:c.8601C>G	NP_000417.2:p.Ser2867=
NM_001079823.1:c.8589C>G	NP_001073291.1:p.Ser2863=
XM_005266981.2:c.8865C>G	XP_005267038.1:p.Ser2955=
XM_005266982.2:c.8853C>G	XP_005267039.1:p.Ser2951=
XM_011535820.1:c.8859C>G	XP_011534122.1:p.Ser2953=
XR_942984.1:n.1461-2462G>C
XR_942985.1:n.1325-2462G>C
XM_005266981.3:c.8865C>G	XP_005267038.1:p.Ser2955=
XM_005266982.3:c.8853C>G	XP_005267039.1:p.Ser2951=
XM_011535820.2:c.8859C>G	XP_011534122.1:p.Ser2953=
XM_017010851.2:c.8871C>G	XP_016866340.1:p.Ser2957=
XM_017010852.1:c.6996C>G	XP_016866341.1:p.Ser2332=
XR_001743859.1:n.3901-2462G>C
XR_001743860.1:n.1180-2462G>C
XR_001743861.1:n.1347-2462G>C
XR_001743863.1:n.883-2462G>C
XR_002956395.1:n.9132-2462G>C
XR_002956396.1:n.3127-2462G>C
NM_000426.4:c.8601C>G MANE Select	NP_000417.3:p.Ser2867=
NM_001079823.2:c.8589C>G	NP_001073291.2:p.Ser2863=