Canonical Allele Identifier: CA365661819
Gene: ENPP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.132172357A>G (hg19) chr6:g.131851217A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851217A>G , CM000668.2:g.131851217A>G GRCh38
NC_000006.11:g.132172357A>G , CM000668.1:g.132172357A>G GRCh37
NC_000006.10:g.132214050A>G NCBI36
NG_008206.1:g.48202A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.506A>G MANE Select ENSP00000498074.1:p.Asp169Gly
ENST00000650147.1:c.184A>G
ENST00000650437.1:c.108+1111A>G
ENST00000360971.6:c.506A>G ENSP00000354238.2:p.Asp169Gly
ENST00000486853.1:n.526A>G
ENST00000513998.5:c.506A>G ENSP00000422424.1:p.Asp169Gly
NM_006208.2:c.506A>G NP_006199.2:p.Asp169Gly
NM_006208.3:c.506A>G MANE Select NP_006199.2:p.Asp169Gly
Search 100 bp 5'
Search 100 bp 3'