Canonical Allele Identifier: CA2282694444
Gene: LAMA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015435A= , CM000680.2:g.7015435A= GRCh38
NC_000018.9:g.7015434A= , CM000680.1:g.7015434A= GRCh37
NC_000018.8:g.7005434A= NCBI36
NG_034251.1:g.107380T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389658.4:c.3126+287T= MANE Select ENSP00000374309.3:n.3126+287T=
ENST00000389658.3:c.3126+287T= ENSP00000374309.3:n.3126+287T=
ENST00000579014.5:n.4141+287T=
NM_005559.3:c.3126+287T= NP_005550.2:n.3126+287T=
XM_011525655.1:c.3126+287T= XP_011523957.1:n.3126+287T=
XM_011525656.1:c.1554+287T= XP_011523958.1:n.1554+287T=
XM_011525657.1:c.3126+287T= XP_011523959.1:n.3126+287T=
XM_011525655.2:c.3126+287T= XP_011523957.1:n.3126+287T=
XM_011525656.2:c.1554+287T= XP_011523958.1:n.1554+287T=
NM_005559.4:c.3126+287T= MANE Select NP_005550.2:n.3126+287T=
Search 100 bp 5'
Search 100 bp 3'