Canonical Allele Identifier: CA2640920058
Gene: LAMA1 HGNC NCBI

Linked Data

gnomAD v4: 18-7015577-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015577G>T , CM000680.2:g.7015577G>T GRCh38
NC_000018.9:g.7015576G>T , CM000680.1:g.7015576G>T GRCh37
NC_000018.8:g.7005576G>T NCBI36
NG_034251.1:g.107238C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000389658.4:c.3126+145C>A MANE Select ENSP00000374309.3:n.3126+145C>A
ENST00000389658.3:c.3126+145C>A ENSP00000374309.3:n.3126+145C>A
ENST00000579014.5:n.4141+145C>A
NM_005559.3:c.3126+145C>A NP_005550.2:n.3126+145C>A
XM_011525655.1:c.3126+145C>A XP_011523957.1:n.3126+145C>A
XM_011525656.1:c.1554+145C>A XP_011523958.1:n.1554+145C>A
XM_011525657.1:c.3126+145C>A XP_011523959.1:n.3126+145C>A
XM_011525655.2:c.3126+145C>A XP_011523957.1:n.3126+145C>A
XM_011525656.2:c.1554+145C>A XP_011523958.1:n.1554+145C>A
NM_005559.4:c.3126+145C>A MANE Select NP_005550.2:n.3126+145C>A