Canonical Allele Identifier: CA2282706886
Gene: LAMA1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7042084T= , CM000680.2:g.7042084T= GRCh38
NC_000018.9:g.7042083T= , CM000680.1:g.7042083T= GRCh37
NC_000018.8:g.7032083T= NCBI36
NG_034251.1:g.80731A=

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.1261+61A= MANE Select ENSP00000374309.3:n.1261+61A=
ENST00000389658.3:c.1261+61A= ENSP00000374309.3:n.1261+61A=
ENST00000579014.5:n.2276+61A=
NM_005559.3:c.1261+61A= NP_005550.2:n.1261+61A=
XM_011525655.1:c.1261+61A= XP_011523957.1:n.1261+61A=
XM_011525657.1:c.1261+61A= XP_011523959.1:n.1261+61A=
XM_011525655.2:c.1261+61A= XP_011523957.1:n.1261+61A=
NM_005559.4:c.1261+61A= MANE Select NP_005550.2:n.1261+61A=
Search 100 bp 5'
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