Canonical Allele Identifier: CA1664251857
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846707_131846709delinsAAC , CM000668.2:g.131846707_131846709delinsAAC GRCh38
NC_000006.11:g.132167847_132167849delinsAAC , CM000668.1:g.132167847_132167849delinsAAC GRCh37
NC_000006.10:g.132209540_132209542delinsAAC NCBI36
NG_008206.1:g.43692_43694delinsAAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000684147.1:n.519-1069_519-1067delinsAAC
ENST00000647893.1:c.241-1069_241-1067delinsAAC MANE Select ENSP00000498074.1:n.241-1069_241-1067delinsAAC
ENST00000650507.1:c.248-1069_248-1067delinsAAC ENSP00000497375.1:n.248-1069_248-1067delinsAAC
ENST00000360971.6:c.241-1069_241-1067delinsAAC ENSP00000354238.2:n.241-1069_241-1067delinsAAC
ENST00000486853.1:n.261-1069_261-1067delinsAAC
ENST00000513998.5:c.241-1069_241-1067delinsAAC ENSP00000422424.1:n.241-1069_241-1067delinsAAC
NM_006208.2:c.241-1069_241-1067delinsAAC NP_006199.2:n.241-1069_241-1067delinsAAC
NM_006208.3:c.241-1069_241-1067delinsAAC MANE Select NP_006199.2:n.241-1069_241-1067delinsAAC