Canonical Allele Identifier: CA651033857
Gene: LAMA4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112136271dup , CM000668.2:g.112136271dup GRCh38
NC_000006.11:g.112457473dup , CM000668.1:g.112457473dup GRCh37
NC_000006.10:g.112564166dup NCBI36
NG_008209.1:g.123357dup , LRG_433:g.123357dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000230538.12:c.3283-16dup MANE Select ENSP00000230538.7:n.3283-16dup
ENST00000389463.9:c.3262-16dup ENSP00000374114.4:n.3262-16dup
ENST00000651860.1:c.1153-16dup ENSP00000498842.1:n.1153-16dup
ENST00000230538.11:c.3283-16dup ENSP00000230538.7:n.3283-16dup
ENST00000389463.8:c.3262-16dup ENSP00000374114.4:n.3262-16dup
ENST00000424408.6:c.3262-16dup ENSP00000416470.2:n.3262-16dup
ENST00000519245.1:n.158-16dup
ENST00000522006.5:c.3262-16dup ENSP00000429488.1:n.3262-16dup
NM_001105206.2:c.3283-16dup NP_001098676.2:n.3283-16dup
NM_001105207.2:c.3262-16dup NP_001098677.2:n.3262-16dup
NM_002290.4:c.3262-16dup NP_002281.3:n.3262-16dup
XM_005266983.3:c.3283-16dup XP_005267040.2:n.3283-16dup
XM_005266984.3:c.3283-16dup XP_005267041.2:n.3283-16dup
XM_011535821.1:c.3283-16dup XP_011534123.1:n.3283-16dup
XM_005266983.4:c.3283-16dup XP_005267040.2:n.3283-16dup
XM_005266984.4:c.3283-16dup XP_005267041.2:n.3283-16dup
XM_017010854.2:c.3262-16dup XP_016866343.1:n.3262-16dup
XR_001743406.2:n.3554-16dup
XR_001743407.2:n.3533-16dup
XR_001744299.1:n.429-19049dup
NM_001105206.3:c.3283-16dup MANE Select NP_001098676.2:n.3283-16dup
NM_001105207.3:c.3262-16dup NP_001098677.2:n.3262-16dup
NM_002290.5:c.3262-16dup NP_002281.3:n.3262-16dup