Canonical Allele Identifier: CA2773039166

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516034_129516039del , CM000668.2:g.129516034_129516039del	GRCh38
NC_000006.11:g.129837179_129837184del , CM000668.1:g.129837179_129837184del	GRCh37
NC_000006.10:g.129878872_129878877del	NCBI36
NG_008678.1:g.637894_637899del , LRG_409:g.637894_637899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-156_1277-151del	ENSP00000510626.1:n.1277-156_1277-151del
ENST00000498257.6:c.1277-156_1277-151del	ENSP00000510533.1:n.1277-156_1277-151del
ENST00000617695.5:c.9200-156_9200-151del	ENSP00000481744.2:n.9200-156_9200-151del
ENST00000618192.5:c.9476-156_9476-151del	ENSP00000480802.2:n.9476-156_9476-151del
ENST00000688198.1:n.2190-156_2190-151del
ENST00000688799.1:c.1277-156_1277-151del	ENSP00000508458.1:n.1277-156_1277-151del
ENST00000690858.1:n.4085-156_4085-151del
ENST00000693461.1:n.1549-156_1549-151del
ENST00000421865.3:c.9212-156_9212-151del MANE Select	ENSP00000400365.2:n.9212-156_9212-151del
ENST00000421865.2:c.9212-156_9212-151del	ENSP00000400365.2:n.9212-156_9212-151del
ENST00000617695.4:c.9200-156_9200-151del	ENSP00000481744.1:n.9200-156_9200-151del
ENST00000618192.4:c.9209-156_9209-151del	ENSP00000480802.1:n.9209-156_9209-151del
NM_000426.3:c.9212-156_9212-151del , LRG_409t1:c.9212-156_9212-151del	NP_000417.2:n.9212-156_9212-151del
NM_001079823.1:c.9200-156_9200-151del	NP_001073291.1:n.9200-156_9200-151del
XM_005266981.2:c.9476-156_9476-151del	XP_005267038.1:n.9476-156_9476-151del
XM_005266982.2:c.9464-156_9464-151del	XP_005267039.1:n.9464-156_9464-151del
XM_011535820.1:c.9470-156_9470-151del	XP_011534122.1:n.9470-156_9470-151del
XR_942984.1:n.1460+6438_1460+6443del
XR_942985.1:n.1324+6438_1324+6443del
XM_005266981.3:c.9476-156_9476-151del	XP_005267038.1:n.9476-156_9476-151del
XM_005266982.3:c.9464-156_9464-151del	XP_005267039.1:n.9464-156_9464-151del
XM_011535820.2:c.9470-156_9470-151del	XP_011534122.1:n.9470-156_9470-151del
XM_017010851.2:c.9482-156_9482-151del	XP_016866340.1:n.9482-156_9482-151del
XM_017010852.1:c.7607-156_7607-151del	XP_016866341.1:n.7607-156_7607-151del
XR_001743859.1:n.3900+6438_3900+6443del
XR_001743860.1:n.1179+6438_1179+6443del
XR_001743861.1:n.1346+6438_1346+6443del
XR_001743863.1:n.883-13248_883-13243del
XR_002956395.1:n.9131+6438_9131+6443del
XR_002956396.1:n.3126+6438_3126+6443del
NM_000426.4:c.9212-156_9212-151del MANE Select	NP_000417.3:n.9212-156_9212-151del
NM_001079823.2:c.9200-156_9200-151del	NP_001073291.2:n.9200-156_9200-151del