Canonical Allele Identifier: CA2282706880
Gene: LAMA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7042076C= , CM000680.2:g.7042076C= GRCh38
NC_000018.9:g.7042075C= , CM000680.1:g.7042075C= GRCh37
NC_000018.8:g.7032075C= NCBI36
NG_034251.1:g.80739G=

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.1261+69G= MANE Select ENSP00000374309.3:n.1261+69G=
ENST00000389658.3:c.1261+69G= ENSP00000374309.3:n.1261+69G=
ENST00000579014.5:n.2276+69G=
NM_005559.3:c.1261+69G= NP_005550.2:n.1261+69G=
XM_011525655.1:c.1261+69G= XP_011523957.1:n.1261+69G=
XM_011525657.1:c.1261+69G= XP_011523959.1:n.1261+69G=
XM_011525655.2:c.1261+69G= XP_011523957.1:n.1261+69G=
NM_005559.4:c.1261+69G= MANE Select NP_005550.2:n.1261+69G=
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