Canonical Allele Identifier: CA502489984
Gene: LAMA1 HGNC NCBI

Linked Data

gnomAD v4: 18-7015731-C-T
MyVariant Identifiers: chr18:g.7015730C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015731C>T , CM000680.2:g.7015731C>T GRCh38
NC_000018.9:g.7015730C>T , CM000680.1:g.7015730C>T GRCh37
NC_000018.8:g.7005730C>T NCBI36
NG_034251.1:g.107084G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.3117G>A MANE Select ENSP00000374309.3:p.Val1039=
ENST00000389658.3:c.3117G>A ENSP00000374309.3:p.Val1039=
ENST00000579014.5:n.4132G>A
NM_005559.3:c.3117G>A NP_005550.2:p.Val1039=
XM_011525655.1:c.3117G>A XP_011523957.1:p.Val1039=
XM_011525656.1:c.1545G>A XP_011523958.1:p.Val515=
XM_011525657.1:c.3117G>A XP_011523959.1:p.Val1039=
XM_011525655.2:c.3117G>A XP_011523957.1:p.Val1039=
XM_011525656.2:c.1545G>A XP_011523958.1:p.Val515=
NM_005559.4:c.3117G>A MANE Select NP_005550.2:p.Val1039=