Canonical Allele Identifier: CA2580074793

Gene: LAMA4

Linked Data

• ClinVar Variation Id: 2098557
• ClinVar RCV Id: RCV003019222

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112109565_112109593del , CM000668.2:g.112109565_112109593del	GRCh38
NC_000006.11:g.112430768_112430796del , CM000668.1:g.112430768_112430796del	GRCh37
NC_000006.10:g.112537461_112537489del	NCBI36
NG_008209.1:g.150036_150064del , LRG_433:g.150036_150064del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000230538.12:c.5327-8_5347del
ENST00000389463.9:c.5306-8_5326del
ENST00000651529.1:c.1345-8_1365del
ENST00000651860.1:c.3050-8_3070del
ENST00000230538.11:c.5327-8_5347del
ENST00000389463.8:c.5306-8_5326del
ENST00000424408.6:c.5306-8_5326del
ENST00000522006.5:c.5306-8_5326del
NM_001105206.2:c.5327-8_5347del
NM_001105207.2:c.5306-8_5326del
NM_002290.4:c.5306-8_5326del
XM_005266983.3:c.5327-8_5347del
XM_005266984.3:c.5327-8_5347del
XM_005266983.4:c.5327-8_5347del
XM_005266984.4:c.5327-8_5347del
XM_017010854.2:c.5306-8_5326del
XR_001743406.2:n.5464-8_5484del
XR_001743407.2:n.5443-8_5463del
NM_001105206.3:c.5327-8_5347del
NM_001105207.3:c.5306-8_5326del
NM_002290.5:c.5306-8_5326del