Canonical Allele Identifier: CA1663194911

Gene: LAMA2

Linked Data

• dbSNP Id: rs1787036688

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516016_129516019dup , CM000668.2:g.129516016_129516019dup	GRCh38
NC_000006.11:g.129837161_129837164dup , CM000668.1:g.129837161_129837164dup	GRCh37
NC_000006.10:g.129878854_129878857dup	NCBI36
NG_008678.1:g.637876_637879dup , LRG_409:g.637876_637879dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-174_1277-171dup	ENSP00000510626.1:n.1277-174_1277-171dup
ENST00000498257.6:c.1277-174_1277-171dup	ENSP00000510533.1:n.1277-174_1277-171dup
ENST00000617695.5:c.9200-174_9200-171dup	ENSP00000481744.2:n.9200-174_9200-171dup
ENST00000618192.5:c.9476-174_9476-171dup	ENSP00000480802.2:n.9476-174_9476-171dup
ENST00000688198.1:n.2190-174_2190-171dup
ENST00000688799.1:c.1277-174_1277-171dup	ENSP00000508458.1:n.1277-174_1277-171dup
ENST00000690858.1:n.4085-174_4085-171dup
ENST00000693461.1:n.1549-174_1549-171dup
ENST00000421865.3:c.9212-174_9212-171dup MANE Select	ENSP00000400365.2:n.9212-174_9212-171dup
ENST00000421865.2:c.9212-174_9212-171dup	ENSP00000400365.2:n.9212-174_9212-171dup
ENST00000617695.4:c.9200-174_9200-171dup	ENSP00000481744.1:n.9200-174_9200-171dup
ENST00000618192.4:c.9209-174_9209-171dup	ENSP00000480802.1:n.9209-174_9209-171dup
NM_000426.3:c.9212-174_9212-171dup , LRG_409t1:c.9212-174_9212-171dup	NP_000417.2:n.9212-174_9212-171dup
NM_001079823.1:c.9200-174_9200-171dup	NP_001073291.1:n.9200-174_9200-171dup
XM_005266981.2:c.9476-174_9476-171dup	XP_005267038.1:n.9476-174_9476-171dup
XM_005266982.2:c.9464-174_9464-171dup	XP_005267039.1:n.9464-174_9464-171dup
XM_011535820.1:c.9470-174_9470-171dup	XP_011534122.1:n.9470-174_9470-171dup
XR_942984.1:n.1460+6459_1460+6462dup
XR_942985.1:n.1324+6459_1324+6462dup
XM_005266981.3:c.9476-174_9476-171dup	XP_005267038.1:n.9476-174_9476-171dup
XM_005266982.3:c.9464-174_9464-171dup	XP_005267039.1:n.9464-174_9464-171dup
XM_011535820.2:c.9470-174_9470-171dup	XP_011534122.1:n.9470-174_9470-171dup
XM_017010851.2:c.9482-174_9482-171dup	XP_016866340.1:n.9482-174_9482-171dup
XM_017010852.1:c.7607-174_7607-171dup	XP_016866341.1:n.7607-174_7607-171dup
XR_001743859.1:n.3900+6459_3900+6462dup
XR_001743860.1:n.1179+6459_1179+6462dup
XR_001743861.1:n.1346+6459_1346+6462dup
XR_001743863.1:n.883-13227_883-13224dup
XR_002956395.1:n.9131+6459_9131+6462dup
XR_002956396.1:n.3126+6459_3126+6462dup
NM_000426.4:c.9212-174_9212-171dup MANE Select	NP_000417.3:n.9212-174_9212-171dup
NM_001079823.2:c.9200-174_9200-171dup	NP_001073291.2:n.9200-174_9200-171dup