Canonical Allele Identifier: CA365634165

Gene: LAMA2

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129503188A>G , CM000668.2:g.129503188A>G	GRCh38
NC_000006.11:g.129824333A>G , CM000668.1:g.129824333A>G	GRCh37
NC_000006.10:g.129866026A>G	NCBI36
NG_008678.1:g.625048A>G , LRG_409:g.625048A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.520A>G	ENSP00000510626.1:p.Arg174Gly
ENST00000498257.6:c.520A>G	ENSP00000510533.1:p.Arg174Gly
ENST00000617695.5:c.8443A>G	ENSP00000481744.2:p.Arg2815Gly
ENST00000618192.5:c.8719A>G	ENSP00000480802.2:p.Arg2907Gly
ENST00000688198.1:n.1433A>G
ENST00000688799.1:c.520A>G	ENSP00000508458.1:p.Arg174Gly
ENST00000690858.1:n.1449A>G
ENST00000693461.1:n.792A>G
ENST00000421865.3:c.8455A>G MANE Select	ENSP00000400365.2:p.Arg2819Gly
ENST00000421865.2:c.8455A>G	ENSP00000400365.2:p.Arg2819Gly
ENST00000617695.4:c.8443A>G	ENSP00000481744.1:p.Arg2815Gly
ENST00000618192.4:c.8452A>G	ENSP00000480802.1:p.Arg2818Gly
NM_000426.3:c.8455A>G , LRG_409t1:c.8455A>G	NP_000417.2:p.Arg2819Gly
NM_001079823.1:c.8443A>G	NP_001073291.1:p.Arg2815Gly
XM_005266981.2:c.8719A>G	XP_005267038.1:p.Arg2907Gly
XM_005266982.2:c.8707A>G	XP_005267039.1:p.Arg2903Gly
XM_011535820.1:c.8713A>G	XP_011534122.1:p.Arg2905Gly
XR_942984.1:n.1461-397T>C
XR_942985.1:n.1325-397T>C
XM_005266981.3:c.8719A>G	XP_005267038.1:p.Arg2907Gly
XM_005266982.3:c.8707A>G	XP_005267039.1:p.Arg2903Gly
XM_011535820.2:c.8713A>G	XP_011534122.1:p.Arg2905Gly
XM_017010851.2:c.8725A>G	XP_016866340.1:p.Arg2909Gly
XM_017010852.1:c.6850A>G	XP_016866341.1:p.Arg2284Gly
XR_001743859.1:n.3901-397T>C
XR_001743860.1:n.1180-397T>C
XR_001743861.1:n.1347-397T>C
XR_001743863.1:n.883-397T>C
XR_002956395.1:n.9132-397T>C
XR_002956396.1:n.3127-397T>C
NM_000426.4:c.8455A>G MANE Select	NP_000417.3:p.Arg2819Gly
NM_001079823.2:c.8443A>G	NP_001073291.2:p.Arg2815Gly