Canonical Allele Identifier: CA295410

Gene: LAMA2

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129514529C>G , CM000668.2:g.129514529C>G	GRCh38
NC_000006.11:g.129835674C>G , CM000668.1:g.129835674C>G	GRCh37
NC_000006.10:g.129877367C>G	NCBI36
NG_008678.1:g.636389C>G , LRG_409:g.636389C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1210C>G	ENSP00000510626.1:p.Gln404Glu
ENST00000498257.6:c.1210C>G	ENSP00000510533.1:p.Gln404Glu
ENST00000617695.5:c.9133C>G	ENSP00000481744.2:p.Gln3045Glu
ENST00000618192.5:c.9409C>G	ENSP00000480802.2:p.Gln3137Glu
ENST00000688198.1:n.2123C>G
ENST00000688799.1:c.1210C>G	ENSP00000508458.1:p.Gln404Glu
ENST00000690858.1:n.4018C>G
ENST00000693461.1:n.1482C>G
ENST00000421865.3:c.9145C>G MANE Select	ENSP00000400365.2:p.Gln3049Glu
ENST00000421865.2:c.9145C>G	ENSP00000400365.2:p.Gln3049Glu
ENST00000617695.4:c.9133C>G	ENSP00000481744.1:p.Gln3045Glu
ENST00000618192.4:c.9142C>G	ENSP00000480802.1:p.Gln3048Glu
NM_000426.3:c.9145C>G , LRG_409t1:c.9145C>G	NP_000417.2:p.Gln3049Glu
NM_001079823.1:c.9133C>G	NP_001073291.1:p.Gln3045Glu
XM_005266981.2:c.9409C>G	XP_005267038.1:p.Gln3137Glu
XM_005266982.2:c.9397C>G	XP_005267039.1:p.Gln3133Glu
XM_011535820.1:c.9403C>G	XP_011534122.1:p.Gln3135Glu
XR_942984.1:n.1460+7948G>C
XR_942985.1:n.1324+7948G>C
XM_005266981.3:c.9409C>G	XP_005267038.1:p.Gln3137Glu
XM_005266982.3:c.9397C>G	XP_005267039.1:p.Gln3133Glu
XM_011535820.2:c.9403C>G	XP_011534122.1:p.Gln3135Glu
XM_017010851.2:c.9415C>G	XP_016866340.1:p.Gln3139Glu
XM_017010852.1:c.7540C>G	XP_016866341.1:p.Gln2514Glu
XR_001743859.1:n.3900+7948G>C
XR_001743860.1:n.1179+7948G>C
XR_001743861.1:n.1346+7948G>C
XR_001743863.1:n.883-11738G>C
XR_002956395.1:n.9131+7948G>C
XR_002956396.1:n.3126+7948G>C
NM_000426.4:c.9145C>G MANE Select	NP_000417.3:p.Gln3049Glu
NM_001079823.2:c.9133C>G	NP_001073291.2:p.Gln3045Glu