Canonical Allele Identifier: CA365660949
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1781875434

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851148T>G , CM000668.2:g.131851148T>G GRCh38
NC_000006.11:g.132172288T>G , CM000668.1:g.132172288T>G GRCh37
NC_000006.10:g.132213981T>G NCBI36
NG_008206.1:g.48133T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.437T>G MANE Select ENSP00000498074.1:p.Ile146Arg
ENST00000650147.1:c.115T>G
ENST00000650437.1:c.108+1042T>G
ENST00000360971.6:c.437T>G ENSP00000354238.2:p.Ile146Arg
ENST00000486853.1:n.457T>G
ENST00000513998.5:c.437T>G ENSP00000422424.1:p.Ile146Arg
NM_006208.2:c.437T>G NP_006199.2:p.Ile146Arg
NM_006208.3:c.437T>G MANE Select NP_006199.2:p.Ile146Arg