Canonical Allele Identifier: CA1663194967

Gene: LAMA2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.129516119_129516120delinsCT , CM000668.2:g.129516119_129516120delinsCT	GRCh38
NC_000006.11:g.129837264_129837265delinsCT , CM000668.1:g.129837264_129837265delinsCT	GRCh37
NC_000006.10:g.129878957_129878958delinsCT	NCBI36
NG_008678.1:g.637979_637980delinsCT , LRG_409:g.637979_637980delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000494137.2:c.1277-71_1277-70delinsCT	ENSP00000510626.1:n.1277-71_1277-70delinsCT
ENST00000498257.6:c.1277-71_1277-70delinsCT	ENSP00000510533.1:n.1277-71_1277-70delinsCT
ENST00000617695.5:c.9200-71_9200-70delinsCT	ENSP00000481744.2:n.9200-71_9200-70delinsCT
ENST00000618192.5:c.9476-71_9476-70delinsCT	ENSP00000480802.2:n.9476-71_9476-70delinsCT
ENST00000688198.1:n.2190-71_2190-70delinsCT
ENST00000688799.1:c.1277-71_1277-70delinsCT	ENSP00000508458.1:n.1277-71_1277-70delinsCT
ENST00000690858.1:n.4085-71_4085-70delinsCT
ENST00000693461.1:n.1549-71_1549-70delinsCT
ENST00000421865.3:c.9212-71_9212-70delinsCT MANE Select	ENSP00000400365.2:n.9212-71_9212-70delinsCT
ENST00000421865.2:c.9212-71_9212-70delinsCT	ENSP00000400365.2:n.9212-71_9212-70delinsCT
ENST00000617695.4:c.9200-71_9200-70delinsCT	ENSP00000481744.1:n.9200-71_9200-70delinsCT
ENST00000618192.4:c.9209-71_9209-70delinsCT	ENSP00000480802.1:n.9209-71_9209-70delinsCT
NM_000426.3:c.9212-71_9212-70delinsCT , LRG_409t1:c.9212-71_9212-70delinsCT	NP_000417.2:n.9212-71_9212-70delinsCT
NM_001079823.1:c.9200-71_9200-70delinsCT	NP_001073291.1:n.9200-71_9200-70delinsCT
XM_005266981.2:c.9476-71_9476-70delinsCT	XP_005267038.1:n.9476-71_9476-70delinsCT
XM_005266982.2:c.9464-71_9464-70delinsCT	XP_005267039.1:n.9464-71_9464-70delinsCT
XM_011535820.1:c.9470-71_9470-70delinsCT	XP_011534122.1:n.9470-71_9470-70delinsCT
XR_942984.1:n.1460+6357_1460+6358delinsAG
XR_942985.1:n.1324+6357_1324+6358delinsAG
XM_005266981.3:c.9476-71_9476-70delinsCT	XP_005267038.1:n.9476-71_9476-70delinsCT
XM_005266982.3:c.9464-71_9464-70delinsCT	XP_005267039.1:n.9464-71_9464-70delinsCT
XM_011535820.2:c.9470-71_9470-70delinsCT	XP_011534122.1:n.9470-71_9470-70delinsCT
XM_017010851.2:c.9482-71_9482-70delinsCT	XP_016866340.1:n.9482-71_9482-70delinsCT
XM_017010852.1:c.7607-71_7607-70delinsCT	XP_016866341.1:n.7607-71_7607-70delinsCT
XR_001743859.1:n.3900+6357_3900+6358delinsAG
XR_001743860.1:n.1179+6357_1179+6358delinsAG
XR_001743861.1:n.1346+6357_1346+6358delinsAG
XR_001743863.1:n.883-13329_883-13328delinsAG
XR_002956395.1:n.9131+6357_9131+6358delinsAG
XR_002956396.1:n.3126+6357_3126+6358delinsAG
NM_000426.4:c.9212-71_9212-70delinsCT MANE Select	NP_000417.3:n.9212-71_9212-70delinsCT
NM_001079823.2:c.9200-71_9200-70delinsCT	NP_001073291.2:n.9200-71_9200-70delinsCT