Canonical Allele Identifier: CA502489973
Gene: LAMA1 HGNC NCBI

Linked Data

dbSNP Id: rs1404535230
gnomAD v3: 18-7015728-C-A
gnomAD v4: 18-7015728-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015728C>A , CM000680.2:g.7015728C>A GRCh38
NC_000018.9:g.7015727C>A , CM000680.1:g.7015727C>A GRCh37
NC_000018.8:g.7005727C>A NCBI36
NG_034251.1:g.107087G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.3120G>T MANE Select ENSP00000374309.3:p.Gly1040=
ENST00000389658.3:c.3120G>T ENSP00000374309.3:p.Gly1040=
ENST00000579014.5:n.4135G>T
NM_005559.3:c.3120G>T NP_005550.2:p.Gly1040=
XM_011525655.1:c.3120G>T XP_011523957.1:p.Gly1040=
XM_011525656.1:c.1548G>T XP_011523958.1:p.Gly516=
XM_011525657.1:c.3120G>T XP_011523959.1:p.Gly1040=
XM_011525655.2:c.3120G>T XP_011523957.1:p.Gly1040=
XM_011525656.2:c.1548G>T XP_011523958.1:p.Gly516=
NM_005559.4:c.3120G>T MANE Select NP_005550.2:p.Gly1040=