Canonical Allele Identifier: CA2282694606
Gene: LAMA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015741T= , CM000680.2:g.7015741T= GRCh38
NC_000018.9:g.7015740T= , CM000680.1:g.7015740T= GRCh37
NC_000018.8:g.7005740T= NCBI36
NG_034251.1:g.107074A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000389658.4:c.3107A= MANE Select ENSP00000374309.3:p.Asp1036=
ENST00000389658.3:c.3107A= ENSP00000374309.3:p.Asp1036=
ENST00000579014.5:n.4122A=
NM_005559.3:c.3107A= NP_005550.2:p.Asp1036=
XM_011525655.1:c.3107A= XP_011523957.1:p.Asp1036=
XM_011525656.1:c.1535A= XP_011523958.1:p.Asp512=
XM_011525657.1:c.3107A= XP_011523959.1:p.Asp1036=
XM_011525655.2:c.3107A= XP_011523957.1:p.Asp1036=
XM_011525656.2:c.1535A= XP_011523958.1:p.Asp512=
NM_005559.4:c.3107A= MANE Select NP_005550.2:p.Asp1036=