Canonical Allele Identifier: CA651157952
Gene: ENPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846792C>T , CM000668.2:g.131846792C>T GRCh38
NC_000006.11:g.132167932C>T , CM000668.1:g.132167932C>T GRCh37
NC_000006.10:g.132209625C>T NCBI36
NG_008206.1:g.43777C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-984C>T
ENST00000647893.1:c.241-984C>T MANE Select ENSP00000498074.1:n.241-984C>T
ENST00000650507.1:c.248-984C>T ENSP00000497375.1:n.248-984C>T
ENST00000360971.6:c.241-984C>T ENSP00000354238.2:n.241-984C>T
ENST00000486853.1:n.261-984C>T
ENST00000513998.5:c.241-984C>T ENSP00000422424.1:n.241-984C>T
NM_006208.2:c.241-984C>T NP_006199.2:n.241-984C>T
NM_006208.3:c.241-984C>T MANE Select NP_006199.2:n.241-984C>T