Canonical Allele Identifier: CA1094400794

Gene: LAMA2

Linked Data

• dbSNP Id: rs1787039255
• gnomAD v3: 6-129516024-C-CTTTCTTTCT
• gnomAD v4: 6-129516024-C-CTTTCTTTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516025_129516033dup , CM000668.2:g.129516025_129516033dup	GRCh38
NC_000006.11:g.129837170_129837178dup , CM000668.1:g.129837170_129837178dup	GRCh37
NC_000006.10:g.129878863_129878871dup	NCBI36
NG_008678.1:g.637885_637893dup , LRG_409:g.637885_637893dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-165_1277-157dup	ENSP00000510626.1:n.1277-165_1277-157dup
ENST00000498257.6:c.1277-165_1277-157dup	ENSP00000510533.1:n.1277-165_1277-157dup
ENST00000617695.5:c.9200-165_9200-157dup	ENSP00000481744.2:n.9200-165_9200-157dup
ENST00000618192.5:c.9476-165_9476-157dup	ENSP00000480802.2:n.9476-165_9476-157dup
ENST00000688198.1:n.2190-165_2190-157dup
ENST00000688799.1:c.1277-165_1277-157dup	ENSP00000508458.1:n.1277-165_1277-157dup
ENST00000690858.1:n.4085-165_4085-157dup
ENST00000693461.1:n.1549-165_1549-157dup
ENST00000421865.3:c.9212-165_9212-157dup MANE Select	ENSP00000400365.2:n.9212-165_9212-157dup
ENST00000421865.2:c.9212-165_9212-157dup	ENSP00000400365.2:n.9212-165_9212-157dup
ENST00000617695.4:c.9200-165_9200-157dup	ENSP00000481744.1:n.9200-165_9200-157dup
ENST00000618192.4:c.9209-165_9209-157dup	ENSP00000480802.1:n.9209-165_9209-157dup
NM_000426.3:c.9212-165_9212-157dup , LRG_409t1:c.9212-165_9212-157dup	NP_000417.2:n.9212-165_9212-157dup
NM_001079823.1:c.9200-165_9200-157dup	NP_001073291.1:n.9200-165_9200-157dup
XM_005266981.2:c.9476-165_9476-157dup	XP_005267038.1:n.9476-165_9476-157dup
XM_005266982.2:c.9464-165_9464-157dup	XP_005267039.1:n.9464-165_9464-157dup
XM_011535820.1:c.9470-165_9470-157dup	XP_011534122.1:n.9470-165_9470-157dup
XR_942984.1:n.1460+6444_1460+6452dup
XR_942985.1:n.1324+6444_1324+6452dup
XM_005266981.3:c.9476-165_9476-157dup	XP_005267038.1:n.9476-165_9476-157dup
XM_005266982.3:c.9464-165_9464-157dup	XP_005267039.1:n.9464-165_9464-157dup
XM_011535820.2:c.9470-165_9470-157dup	XP_011534122.1:n.9470-165_9470-157dup
XM_017010851.2:c.9482-165_9482-157dup	XP_016866340.1:n.9482-165_9482-157dup
XM_017010852.1:c.7607-165_7607-157dup	XP_016866341.1:n.7607-165_7607-157dup
XR_001743859.1:n.3900+6444_3900+6452dup
XR_001743860.1:n.1179+6444_1179+6452dup
XR_001743861.1:n.1346+6444_1346+6452dup
XR_001743863.1:n.883-13242_883-13234dup
XR_002956395.1:n.9131+6444_9131+6452dup
XR_002956396.1:n.3126+6444_3126+6452dup
NM_000426.4:c.9212-165_9212-157dup MANE Select	NP_000417.3:n.9212-165_9212-157dup
NM_001079823.2:c.9200-165_9200-157dup	NP_001073291.2:n.9200-165_9200-157dup