Canonical Allele Identifier: CA365637221

Gene: LAMA2

Linked Data

• MyVariant Identifiers: chr6:g.129837352G>C (hg19) ; chr6:g.129516207G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516207G>C , CM000668.2:g.129516207G>C	GRCh38
NC_000006.11:g.129837352G>C , CM000668.1:g.129837352G>C	GRCh37
NC_000006.10:g.129879045G>C	NCBI36
NG_008678.1:g.638067G>C , LRG_409:g.638067G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1294G>C	ENSP00000510626.1:p.Gly432Arg
ENST00000498257.6:c.1294G>C	ENSP00000510533.1:p.Gly432Arg
ENST00000617695.5:c.9217G>C	ENSP00000481744.2:p.Gly3073Arg
ENST00000618192.5:c.9493G>C	ENSP00000480802.2:p.Gly3165Arg
ENST00000688198.1:n.2207G>C
ENST00000688799.1:c.1294G>C	ENSP00000508458.1:p.Gly432Arg
ENST00000690858.1:n.4102G>C
ENST00000693461.1:n.1566G>C
ENST00000421865.3:c.9229G>C MANE Select	ENSP00000400365.2:p.Gly3077Arg
ENST00000421865.2:c.9229G>C	ENSP00000400365.2:p.Gly3077Arg
ENST00000617695.4:c.9217G>C	ENSP00000481744.1:p.Gly3073Arg
ENST00000618192.4:c.9226G>C	ENSP00000480802.1:p.Gly3076Arg
NM_000426.3:c.9229G>C , LRG_409t1:c.9229G>C	NP_000417.2:p.Gly3077Arg
NM_001079823.1:c.9217G>C	NP_001073291.1:p.Gly3073Arg
XM_005266981.2:c.9493G>C	XP_005267038.1:p.Gly3165Arg
XM_005266982.2:c.9481G>C	XP_005267039.1:p.Gly3161Arg
XM_011535820.1:c.9487G>C	XP_011534122.1:p.Gly3163Arg
XR_942984.1:n.1460+6270C>G
XR_942985.1:n.1324+6270C>G
XM_005266981.3:c.9493G>C	XP_005267038.1:p.Gly3165Arg
XM_005266982.3:c.9481G>C	XP_005267039.1:p.Gly3161Arg
XM_011535820.2:c.9487G>C	XP_011534122.1:p.Gly3163Arg
XM_017010851.2:c.9499G>C	XP_016866340.1:p.Gly3167Arg
XM_017010852.1:c.7624G>C	XP_016866341.1:p.Gly2542Arg
XR_001743859.1:n.3900+6270C>G
XR_001743860.1:n.1179+6270C>G
XR_001743861.1:n.1346+6270C>G
XR_001743863.1:n.883-13416C>G
XR_002956395.1:n.9131+6270C>G
XR_002956396.1:n.3126+6270C>G
NM_000426.4:c.9229G>C MANE Select	NP_000417.3:p.Gly3077Arg
NM_001079823.2:c.9217G>C	NP_001073291.2:p.Gly3073Arg