Canonical Allele Identifier: CA365660935
Gene: ENPP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.132172286T>A (hg19) chr6:g.131851146T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851146T>A , CM000668.2:g.131851146T>A GRCh38
NC_000006.11:g.132172286T>A , CM000668.1:g.132172286T>A GRCh37
NC_000006.10:g.132213979T>A NCBI36
NG_008206.1:g.48131T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.435T>A MANE Select ENSP00000498074.1:p.His145Gln
ENST00000650147.1:c.113T>A
ENST00000650437.1:c.108+1040T>A
ENST00000360971.6:c.435T>A ENSP00000354238.2:p.His145Gln
ENST00000486853.1:n.455T>A
ENST00000513998.5:c.435T>A ENSP00000422424.1:p.His145Gln
NM_006208.2:c.435T>A NP_006199.2:p.His145Gln
NM_006208.3:c.435T>A MANE Select NP_006199.2:p.His145Gln
Search 100 bp 5'
Search 100 bp 3'