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UPDATE - Protein Allele ID & Protein Sequence HGVS Requests Partially Restored
Protein allele requests are no longer disabled.
Currently, hypothetical explanatory transcript generation is not part of the response and is being investigated.
ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
CA502473608
Gene: LAMA1
HGNC
NCBI
Linked Data
MyVariant Identifiers:
chr18:g.7042175A>G (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.7042176A>G , CM000680.2:g.7042176A>G
GRCh38
NC_000018.9:g.7042175A>G , CM000680.1:g.7042175A>G
GRCh37
NC_000018.8:g.7032175A>G
NCBI36
NG_034251.1:g.80639T>C
Transcript Alleles
HGVS
Amino-acid change
ENST00000389658.4:c.1230T>C
MANE Select
ENSP00000374309.3:p.Ile410=
ENST00000389658.3:c.1230T>C
ENSP00000374309.3:p.Ile410=
ENST00000579014.5:n.2245T>C
NM_005559.3:c.1230T>C
NP_005550.2:p.Ile410=
XM_011525655.1:c.1230T>C
XP_011523957.1:p.Ile410=
XM_011525657.1:c.1230T>C
XP_011523959.1:p.Ile410=
XM_011525655.2:c.1230T>C
XP_011523957.1:p.Ile410=
NM_005559.4:c.1230T>C
MANE Select
NP_005550.2:p.Ile410=
Search 100 bp 5'
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