Canonical Allele Identifier: CA401836265
Gene: LAMA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.7042175A>C (hg19) chr18:g.7042176A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7042176A>C , CM000680.2:g.7042176A>C GRCh38
NC_000018.9:g.7042175A>C , CM000680.1:g.7042175A>C GRCh37
NC_000018.8:g.7032175A>C NCBI36
NG_034251.1:g.80639T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.1230T>G MANE Select ENSP00000374309.3:p.Ile410Met
ENST00000389658.3:c.1230T>G ENSP00000374309.3:p.Ile410Met
ENST00000579014.5:n.2245T>G
NM_005559.3:c.1230T>G NP_005550.2:p.Ile410Met
XM_011525655.1:c.1230T>G XP_011523957.1:p.Ile410Met
XM_011525657.1:c.1230T>G XP_011523959.1:p.Ile410Met
XM_011525655.2:c.1230T>G XP_011523957.1:p.Ile410Met
NM_005559.4:c.1230T>G MANE Select NP_005550.2:p.Ile410Met
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