Canonical Allele Identifier: CA1663194915

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516022_129516026delinsATCTT , CM000668.2:g.129516022_129516026delinsATCTT	GRCh38
NC_000006.11:g.129837167_129837171delinsATCTT , CM000668.1:g.129837167_129837171delinsATCTT	GRCh37
NC_000006.10:g.129878860_129878864delinsATCTT	NCBI36
NG_008678.1:g.637882_637886delinsATCTT , LRG_409:g.637882_637886delinsATCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-168_1277-164delinsATCTT	ENSP00000510626.1:n.1277-168_1277-164delinsATCTT
ENST00000498257.6:c.1277-168_1277-164delinsATCTT	ENSP00000510533.1:n.1277-168_1277-164delinsATCTT
ENST00000617695.5:c.9200-168_9200-164delinsATCTT	ENSP00000481744.2:n.9200-168_9200-164delinsATCTT
ENST00000618192.5:c.9476-168_9476-164delinsATCTT	ENSP00000480802.2:n.9476-168_9476-164delinsATCTT
ENST00000688198.1:n.2190-168_2190-164delinsATCTT
ENST00000688799.1:c.1277-168_1277-164delinsATCTT	ENSP00000508458.1:n.1277-168_1277-164delinsATCTT
ENST00000690858.1:n.4085-168_4085-164delinsATCTT
ENST00000693461.1:n.1549-168_1549-164delinsATCTT
ENST00000421865.3:c.9212-168_9212-164delinsATCTT MANE Select	ENSP00000400365.2:n.9212-168_9212-164delinsATCTT
ENST00000421865.2:c.9212-168_9212-164delinsATCTT	ENSP00000400365.2:n.9212-168_9212-164delinsATCTT
ENST00000617695.4:c.9200-168_9200-164delinsATCTT	ENSP00000481744.1:n.9200-168_9200-164delinsATCTT
ENST00000618192.4:c.9209-168_9209-164delinsATCTT	ENSP00000480802.1:n.9209-168_9209-164delinsATCTT
NM_000426.3:c.9212-168_9212-164delinsATCTT , LRG_409t1:c.9212-168_9212-164delinsATCTT	NP_000417.2:n.9212-168_9212-164delinsATCTT
NM_001079823.1:c.9200-168_9200-164delinsATCTT	NP_001073291.1:n.9200-168_9200-164delinsATCTT
XM_005266981.2:c.9476-168_9476-164delinsATCTT	XP_005267038.1:n.9476-168_9476-164delinsATCTT
XM_005266982.2:c.9464-168_9464-164delinsATCTT	XP_005267039.1:n.9464-168_9464-164delinsATCTT
XM_011535820.1:c.9470-168_9470-164delinsATCTT	XP_011534122.1:n.9470-168_9470-164delinsATCTT
XR_942984.1:n.1460+6451_1460+6455delinsAAGAT
XR_942985.1:n.1324+6451_1324+6455delinsAAGAT
XM_005266981.3:c.9476-168_9476-164delinsATCTT	XP_005267038.1:n.9476-168_9476-164delinsATCTT
XM_005266982.3:c.9464-168_9464-164delinsATCTT	XP_005267039.1:n.9464-168_9464-164delinsATCTT
XM_011535820.2:c.9470-168_9470-164delinsATCTT	XP_011534122.1:n.9470-168_9470-164delinsATCTT
XM_017010851.2:c.9482-168_9482-164delinsATCTT	XP_016866340.1:n.9482-168_9482-164delinsATCTT
XM_017010852.1:c.7607-168_7607-164delinsATCTT	XP_016866341.1:n.7607-168_7607-164delinsATCTT
XR_001743859.1:n.3900+6451_3900+6455delinsAAGAT
XR_001743860.1:n.1179+6451_1179+6455delinsAAGAT
XR_001743861.1:n.1346+6451_1346+6455delinsAAGAT
XR_001743863.1:n.883-13235_883-13231delinsAAGAT
XR_002956395.1:n.9131+6451_9131+6455delinsAAGAT
XR_002956396.1:n.3126+6451_3126+6455delinsAAGAT
NM_000426.4:c.9212-168_9212-164delinsATCTT MANE Select	NP_000417.3:n.9212-168_9212-164delinsATCTT
NM_001079823.2:c.9200-168_9200-164delinsATCTT	NP_001073291.2:n.9200-168_9200-164delinsATCTT