Canonical Allele Identifier: CA1655234123

Gene: LAMA4

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112147918_112147920delinsACT , CM000668.2:g.112147918_112147920delinsACT	GRCh38
NC_000006.11:g.112469120_112469122delinsACT , CM000668.1:g.112469120_112469122delinsACT	GRCh37
NC_000006.10:g.112575813_112575815delinsACT	NCBI36
NG_008209.1:g.111707_111709delinsAGT , LRG_433:g.111707_111709delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.2353+237_2353+239delinsAGT MANE Select	ENSP00000230538.7:n.2353+237_2353+239delinsAGT
ENST00000389463.9:c.2332+237_2332+239delinsAGT	ENSP00000374114.4:n.2332+237_2332+239delinsAGT
ENST00000651860.1:c.223+237_223+239delinsAGT	ENSP00000498842.1:n.223+237_223+239delinsAGT
ENST00000230538.11:c.2353+237_2353+239delinsAGT	ENSP00000230538.7:n.2353+237_2353+239delinsAGT
ENST00000389463.8:c.2332+237_2332+239delinsAGT	ENSP00000374114.4:n.2332+237_2332+239delinsAGT
ENST00000424408.6:c.2332+237_2332+239delinsAGT	ENSP00000416470.2:n.2332+237_2332+239delinsAGT
ENST00000522006.5:c.2332+237_2332+239delinsAGT	ENSP00000429488.1:n.2332+237_2332+239delinsAGT
ENST00000523765.1:c.765+237_765+239delinsAGT
NM_001105206.2:c.2353+237_2353+239delinsAGT	NP_001098676.2:n.2353+237_2353+239delinsAGT
NM_001105207.2:c.2332+237_2332+239delinsAGT	NP_001098677.2:n.2332+237_2332+239delinsAGT
NM_002290.4:c.2332+237_2332+239delinsAGT	NP_002281.3:n.2332+237_2332+239delinsAGT
XM_005266983.3:c.2353+237_2353+239delinsAGT	XP_005267040.2:n.2353+237_2353+239delinsAGT
XM_005266984.3:c.2353+237_2353+239delinsAGT	XP_005267041.2:n.2353+237_2353+239delinsAGT
XM_011535821.1:c.2353+237_2353+239delinsAGT	XP_011534123.1:n.2353+237_2353+239delinsAGT
XM_005266983.4:c.2353+237_2353+239delinsAGT	XP_005267040.2:n.2353+237_2353+239delinsAGT
XM_005266984.4:c.2353+237_2353+239delinsAGT	XP_005267041.2:n.2353+237_2353+239delinsAGT
XM_017010854.2:c.2332+237_2332+239delinsAGT	XP_016866343.1:n.2332+237_2332+239delinsAGT
XR_001743406.2:n.2624+237_2624+239delinsAGT
XR_001743407.2:n.2603+237_2603+239delinsAGT
XR_001744299.1:n.429-7402_429-7400delinsACT
NM_001105206.3:c.2353+237_2353+239delinsAGT MANE Select	NP_001098676.2:n.2353+237_2353+239delinsAGT
NM_001105207.3:c.2332+237_2332+239delinsAGT	NP_001098677.2:n.2332+237_2332+239delinsAGT
NM_002290.5:c.2332+237_2332+239delinsAGT	NP_002281.3:n.2332+237_2332+239delinsAGT