Canonical Allele Identifier: CA401836213
Gene: LAMA1 HGNC NCBI

Linked Data

COSMIC: COSM50454
MyVariant Identifiers: chr18:g.7042168C>T (hg19) chr18:g.7042169C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7042169C>T , CM000680.2:g.7042169C>T GRCh38
NC_000018.9:g.7042168C>T , CM000680.1:g.7042168C>T GRCh37
NC_000018.8:g.7032168C>T NCBI36
NG_034251.1:g.80646G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.1237G>A MANE Select ENSP00000374309.3:p.Asp413Asn
ENST00000389658.3:c.1237G>A ENSP00000374309.3:p.Asp413Asn
ENST00000579014.5:n.2252G>A
NM_005559.3:c.1237G>A NP_005550.2:p.Asp413Asn
XM_011525655.1:c.1237G>A XP_011523957.1:p.Asp413Asn
XM_011525657.1:c.1237G>A XP_011523959.1:p.Asp413Asn
XM_011525655.2:c.1237G>A XP_011523957.1:p.Asp413Asn
NM_005559.4:c.1237G>A MANE Select NP_005550.2:p.Asp413Asn
Search 100 bp 5'
Search 100 bp 3'