Canonical Allele Identifier: CA2517814833

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112148148_112148158del , CM000668.2:g.112148148_112148158del	GRCh38
NC_000006.11:g.112469350_112469360del , CM000668.1:g.112469350_112469360del	GRCh37
NC_000006.10:g.112576043_112576053del	NCBI36
NG_008209.1:g.111471_111481del , LRG_433:g.111471_111481del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.2353+1_2353+11del
ENST00000389463.9:c.2332+1_2332+11del
ENST00000651860.1:c.223+1_223+11del
ENST00000230538.11:c.2353+1_2353+11del
ENST00000389463.8:c.2332+1_2332+11del
ENST00000424408.6:c.2332+1_2332+11del
ENST00000522006.5:c.2332+1_2332+11del
ENST00000523765.1:c.765+1_765+11del
NM_001105206.2:c.2353+1_2353+11del
NM_001105207.2:c.2332+1_2332+11del
NM_002290.4:c.2332+1_2332+11del
XM_005266983.3:c.2353+1_2353+11del
XM_005266984.3:c.2353+1_2353+11del
XM_011535821.1:c.2353+1_2353+11del
XM_005266983.4:c.2353+1_2353+11del
XM_005266984.4:c.2353+1_2353+11del
XM_017010854.2:c.2332+1_2332+11del
XR_001743406.2:n.2624+1_2624+11del
XR_001743407.2:n.2603+1_2603+11del
XR_001744299.1:n.429-7172_429-7162del
NM_001105206.3:c.2353+1_2353+11del
NM_001105207.3:c.2332+1_2332+11del
NM_002290.5:c.2332+1_2332+11del