Canonical Allele Identifier: CA2282706925
Gene: LAMA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7042164G= , CM000680.2:g.7042164G= GRCh38
NC_000018.9:g.7042163G= , CM000680.1:g.7042163G= GRCh37
NC_000018.8:g.7032163G= NCBI36
NG_034251.1:g.80651C=

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.1242C= MANE Select ENSP00000374309.3:p.Leu414=
ENST00000389658.3:c.1242C= ENSP00000374309.3:p.Leu414=
ENST00000579014.5:n.2257C=
NM_005559.3:c.1242C= NP_005550.2:p.Leu414=
XM_011525655.1:c.1242C= XP_011523957.1:p.Leu414=
XM_011525657.1:c.1242C= XP_011523959.1:p.Leu414=
XM_011525655.2:c.1242C= XP_011523957.1:p.Leu414=
NM_005559.4:c.1242C= MANE Select NP_005550.2:p.Leu414=