Canonical Allele Identifier: CA452161746
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1347882772
gnomAD v2: 6-132211642-A-G
gnomAD v4: 6-131890502-A-G
MyVariant Identifiers: chr6:g.132211642A>G (hg19) chr6:g.131890502A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890502A>G , CM000668.2:g.131890502A>G GRCh38
NC_000006.11:g.132211642A>G , CM000668.1:g.132211642A>G GRCh37
NC_000006.10:g.132253335A>G NCBI36
NG_008206.1:g.87487A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1200A>G
ENST00000647893.1:c.2769A>G MANE Select ENSP00000498074.1:p.Gln923=
ENST00000360971.6:c.2769A>G ENSP00000354238.2:p.Gln923=
ENST00000513998.5:c.*1606A>G ENSP00000422424.1:n.*1606A>G
NM_006208.2:c.2769A>G NP_006199.2:p.Gln923=
XM_011535896.1:c.1659A>G XP_011534198.1:p.Gln553=
NM_006208.3:c.2769A>G MANE Select NP_006199.2:p.Gln923=
Search 100 bp 5'
Search 100 bp 3'