Canonical Allele Identifier: CA1664283171
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890514_131890515delinsTG , CM000668.2:g.131890514_131890515delinsTG GRCh38
NC_000006.11:g.132211654_132211655delinsTG , CM000668.1:g.132211654_132211655delinsTG GRCh37
NC_000006.10:g.132253347_132253348delinsTG NCBI36
NG_008206.1:g.87499_87500delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1212_1213delinsTG
ENST00000647893.1:c.*3_*4delinsTG MANE Select ENSP00000498074.1:n.*3_*4delinsTG
ENST00000360971.6:c.*3_*4delinsTG ENSP00000354238.2:n.*3_*4delinsTG
ENST00000513998.5:c.*1618_*1619delinsTG ENSP00000422424.1:n.*1618_*1619delinsTG
NM_006208.2:c.*3_*4delinsTG NP_006199.2:n.*3_*4delinsTG
XM_011535896.1:c.*3_*4delinsTG XP_011534198.1:n.*3_*4delinsTG
NM_006208.3:c.*3_*4delinsTG MANE Select NP_006199.2:n.*3_*4delinsTG