Canonical Allele Identifier: CA401850441
Gene: LAMA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr18:g.7015743T>G (hg19) chr18:g.7015744T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015744T>G , CM000680.2:g.7015744T>G GRCh38
NC_000018.9:g.7015743T>G , CM000680.1:g.7015743T>G GRCh37
NC_000018.8:g.7005743T>G NCBI36
NG_034251.1:g.107071A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389658.4:c.3104A>C MANE Select ENSP00000374309.3:p.Tyr1035Ser
ENST00000389658.3:c.3104A>C ENSP00000374309.3:p.Tyr1035Ser
ENST00000579014.5:n.4119A>C
NM_005559.3:c.3104A>C NP_005550.2:p.Tyr1035Ser
XM_011525655.1:c.3104A>C XP_011523957.1:p.Tyr1035Ser
XM_011525656.1:c.1532A>C XP_011523958.1:p.Tyr511Ser
XM_011525657.1:c.3104A>C XP_011523959.1:p.Tyr1035Ser
XM_011525655.2:c.3104A>C XP_011523957.1:p.Tyr1035Ser
XM_011525656.2:c.1532A>C XP_011523958.1:p.Tyr511Ser
NM_005559.4:c.3104A>C MANE Select NP_005550.2:p.Tyr1035Ser
Search 100 bp 5'
Search 100 bp 3'