Canonical Allele Identifier: CA819059036
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1272856864

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846790A>T , CM000668.2:g.131846790A>T GRCh38
NC_000006.11:g.132167930A>T , CM000668.1:g.132167930A>T GRCh37
NC_000006.10:g.132209623A>T NCBI36
NG_008206.1:g.43775A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-986A>T
ENST00000647893.1:c.241-986A>T MANE Select ENSP00000498074.1:n.241-986A>T
ENST00000650507.1:c.248-986A>T ENSP00000497375.1:n.248-986A>T
ENST00000360971.6:c.241-986A>T ENSP00000354238.2:n.241-986A>T
ENST00000486853.1:n.261-986A>T
ENST00000513998.5:c.241-986A>T ENSP00000422424.1:n.241-986A>T
NM_006208.2:c.241-986A>T NP_006199.2:n.241-986A>T
NM_006208.3:c.241-986A>T MANE Select NP_006199.2:n.241-986A>T