Canonical Allele Identifier: CA365660396
Gene: ENPP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.132211546T>A (hg19) chr6:g.131890406T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890406T>A , CM000668.2:g.131890406T>A GRCh38
NC_000006.11:g.132211546T>A , CM000668.1:g.132211546T>A GRCh37
NC_000006.10:g.132253239T>A NCBI36
NG_008206.1:g.87391T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1104T>A
ENST00000647893.1:c.2673T>A MANE Select ENSP00000498074.1:p.Asp891Glu
ENST00000360971.6:c.2673T>A ENSP00000354238.2:p.Asp891Glu
ENST00000513998.5:c.*1510T>A ENSP00000422424.1:n.*1510T>A
NM_006208.2:c.2673T>A NP_006199.2:p.Asp891Glu
XM_011535896.1:c.1563T>A XP_011534198.1:p.Asp521Glu
NM_006208.3:c.2673T>A MANE Select NP_006199.2:p.Asp891Glu
Search 100 bp 5'
Search 100 bp 3'