Canonical Allele Identifier: CA2838896551
Gene: LAMA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015892G>T , CM000680.2:g.7015892G>T GRCh38
NC_000018.9:g.7015891G>T , CM000680.1:g.7015891G>T GRCh37
NC_000018.8:g.7005891G>T NCBI36
NG_034251.1:g.106923C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389658.4:c.2990-34C>A MANE Select ENSP00000374309.3:n.2990-34C>A
ENST00000389658.3:c.2990-34C>A ENSP00000374309.3:n.2990-34C>A
ENST00000579014.5:n.4005-34C>A
NM_005559.3:c.2990-34C>A NP_005550.2:n.2990-34C>A
XM_011525655.1:c.2990-34C>A XP_011523957.1:n.2990-34C>A
XM_011525656.1:c.1418-34C>A XP_011523958.1:n.1418-34C>A
XM_011525657.1:c.2990-34C>A XP_011523959.1:n.2990-34C>A
XM_011525655.2:c.2990-34C>A XP_011523957.1:n.2990-34C>A
XM_011525656.2:c.1418-34C>A XP_011523958.1:n.1418-34C>A
NM_005559.4:c.2990-34C>A MANE Select NP_005550.2:n.2990-34C>A