Canonical Allele Identifier: CA1663194922

Gene: LAMA2

Linked Data

• dbSNP Id: rs1787040506

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516033_129516034insTTCTCTACAATTCTATTAGTAAGG , CM000668.2:g.129516033_129516034insTTCTCTACAATTCTATTAGTAAGG	GRCh38
NC_000006.11:g.129837178_129837179insTTCTCTACAATTCTATTAGTAAGG , CM000668.1:g.129837178_129837179insTTCTCTACAATTCTATTAGTAAGG	GRCh37
NC_000006.10:g.129878871_129878872insTTCTCTACAATTCTATTAGTAAGG	NCBI36
NG_008678.1:g.637893_637894insTTCTCTACAATTCTATTAGTAAGG , LRG_409:g.637893_637894insTTCTCTACAATTCTATTAGTAAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-157_1277-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000510626.1:n.1277-157_1277-156insTTCTCTACAATTCTATTAGTA...
ENST00000498257.6:c.1277-157_1277-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000510533.1:n.1277-157_1277-156insTTCTCTACAATTCTATTAGTA...
ENST00000617695.5:c.9200-157_9200-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000481744.2:n.9200-157_9200-156insTTCTCTACAATTCTATTAGTA...
ENST00000618192.5:c.9476-157_9476-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000480802.2:n.9476-157_9476-156insTTCTCTACAATTCTATTAGTA...
ENST00000688198.1:n.2190-157_2190-156insTTCTCTACAATTCTATTAGTAAGG
ENST00000688799.1:c.1277-157_1277-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000508458.1:n.1277-157_1277-156insTTCTCTACAATTCTATTAGTA...
ENST00000690858.1:n.4085-157_4085-156insTTCTCTACAATTCTATTAGTAAGG
ENST00000693461.1:n.1549-157_1549-156insTTCTCTACAATTCTATTAGTAAGG
ENST00000421865.3:c.9212-157_9212-156insTTCTCTACAATTCTATTAGTAAGG MANE Select	ENSP00000400365.2:n.9212-157_9212-156insTTCTCTACAATTCTATTAGTA...
ENST00000421865.2:c.9212-157_9212-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000400365.2:n.9212-157_9212-156insTTCTCTACAATTCTATTAGTA...
ENST00000617695.4:c.9200-157_9200-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000481744.1:n.9200-157_9200-156insTTCTCTACAATTCTATTAGTA...
ENST00000618192.4:c.9209-157_9209-156insTTCTCTACAATTCTATTAGTAAGG	ENSP00000480802.1:n.9209-157_9209-156insTTCTCTACAATTCTATTAGTA...
NM_000426.3:c.9212-157_9212-156insTTCTCTACAATTCTATTAGTAAGG , LRG_409t1:c.9212-157_9212-156insTTCTCTACAATTCTATTAGTAAGG	NP_000417.2:n.9212-157_9212-156insTTCTCTACAATTCTATTAGTAAGG
NM_001079823.1:c.9200-157_9200-156insTTCTCTACAATTCTATTAGTAAGG	NP_001073291.1:n.9200-157_9200-156insTTCTCTACAATTCTATTAGTAAGG...
XM_005266981.2:c.9476-157_9476-156insTTCTCTACAATTCTATTAGTAAGG	XP_005267038.1:n.9476-157_9476-156insTTCTCTACAATTCTATTAGTAAGG...
XM_005266982.2:c.9464-157_9464-156insTTCTCTACAATTCTATTAGTAAGG	XP_005267039.1:n.9464-157_9464-156insTTCTCTACAATTCTATTAGTAAGG...
XM_011535820.1:c.9470-157_9470-156insTTCTCTACAATTCTATTAGTAAGG	XP_011534122.1:n.9470-157_9470-156insTTCTCTACAATTCTATTAGTAAGG...
XR_942984.1:n.1460+6443_1460+6444insCCTTACTAATAGAATTGTAGAGAA
XR_942985.1:n.1324+6443_1324+6444insCCTTACTAATAGAATTGTAGAGAA
XM_005266981.3:c.9476-157_9476-156insTTCTCTACAATTCTATTAGTAAGG	XP_005267038.1:n.9476-157_9476-156insTTCTCTACAATTCTATTAGTAAGG...
XM_005266982.3:c.9464-157_9464-156insTTCTCTACAATTCTATTAGTAAGG	XP_005267039.1:n.9464-157_9464-156insTTCTCTACAATTCTATTAGTAAGG...
XM_011535820.2:c.9470-157_9470-156insTTCTCTACAATTCTATTAGTAAGG	XP_011534122.1:n.9470-157_9470-156insTTCTCTACAATTCTATTAGTAAGG...
XM_017010851.2:c.9482-157_9482-156insTTCTCTACAATTCTATTAGTAAGG	XP_016866340.1:n.9482-157_9482-156insTTCTCTACAATTCTATTAGTAAGG...
XM_017010852.1:c.7607-157_7607-156insTTCTCTACAATTCTATTAGTAAGG	XP_016866341.1:n.7607-157_7607-156insTTCTCTACAATTCTATTAGTAAGG...
XR_001743859.1:n.3900+6443_3900+6444insCCTTACTAATAGAATTGTAGAGAA
XR_001743860.1:n.1179+6443_1179+6444insCCTTACTAATAGAATTGTAGAGAA
XR_001743861.1:n.1346+6443_1346+6444insCCTTACTAATAGAATTGTAGAGAA
XR_001743863.1:n.883-13243_883-13242insCCTTACTAATAGAATTGTAGAGAA
XR_002956395.1:n.9131+6443_9131+6444insCCTTACTAATAGAATTGTAGAGAA
XR_002956396.1:n.3126+6443_3126+6444insCCTTACTAATAGAATTGTAGAGAA
NM_000426.4:c.9212-157_9212-156insTTCTCTACAATTCTATTAGTAAGG MANE Select	NP_000417.3:n.9212-157_9212-156insTTCTCTACAATTCTATTAGTAAGG
NM_001079823.2:c.9200-157_9200-156insTTCTCTACAATTCTATTAGTAAGG	NP_001073291.2:n.9200-157_9200-156insTTCTCTACAATTCTATTAGTAAGG...