Canonical Allele Identifier: CA1664277025
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131877066T= , CM000668.2:g.131877066T= GRCh38
NC_000006.11:g.132198206T= , CM000668.1:g.132198206T= GRCh37
NC_000006.10:g.132239899T= NCBI36
NG_008206.1:g.74051T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683687.1:n.670T=
ENST00000684536.1:n.296T=
ENST00000647893.1:c.1798T= MANE Select ENSP00000498074.1:p.Tyr600=
ENST00000647981.1:n.483T=
ENST00000650437.1:c.1289T=
ENST00000360971.6:c.1798T= ENSP00000354238.2:p.Tyr600=
ENST00000459624.1:n.842T=
ENST00000513998.5:c.*635T= ENSP00000422424.1:n.*635T=
NM_006208.2:c.1798T= NP_006199.2:p.Tyr600=
XM_011535896.1:c.688T= XP_011534198.1:p.Tyr230=
NM_006208.3:c.1798T= MANE Select NP_006199.2:p.Tyr600=