Canonical Allele Identifier: CA2282694491
Gene: LAMA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015546C= , CM000680.2:g.7015546C= GRCh38
NC_000018.9:g.7015545C= , CM000680.1:g.7015545C= GRCh37
NC_000018.8:g.7005545C= NCBI36
NG_034251.1:g.107269G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389658.4:c.3126+176G= MANE Select ENSP00000374309.3:n.3126+176G=
ENST00000389658.3:c.3126+176G= ENSP00000374309.3:n.3126+176G=
ENST00000579014.5:n.4141+176G=
NM_005559.3:c.3126+176G= NP_005550.2:n.3126+176G=
XM_011525655.1:c.3126+176G= XP_011523957.1:n.3126+176G=
XM_011525656.1:c.1554+176G= XP_011523958.1:n.1554+176G=
XM_011525657.1:c.3126+176G= XP_011523959.1:n.3126+176G=
XM_011525655.2:c.3126+176G= XP_011523957.1:n.3126+176G=
XM_011525656.2:c.1554+176G= XP_011523958.1:n.1554+176G=
NM_005559.4:c.3126+176G= MANE Select NP_005550.2:n.3126+176G=
Search 100 bp 5'
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