Canonical Allele Identifier: CA1664283198
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890555_131890562delinsCTTATATT , CM000668.2:g.131890555_131890562delinsCTTATATT GRCh38
NC_000006.11:g.132211695_132211702delinsCTTATATT , CM000668.1:g.132211695_132211702delinsCTTATATT GRCh37
NC_000006.10:g.132253388_132253395delinsCTTATATT NCBI36
NG_008206.1:g.87540_87547delinsCTTATATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1253_1260delinsCTTATATT
ENST00000647893.1:c.*44_*51delinsCTTATATT MANE Select ENSP00000498074.1:n.*44_*51delinsCTTATATT
ENST00000360971.6:c.*44_*51delinsCTTATATT ENSP00000354238.2:n.*44_*51delinsCTTATATT
ENST00000513998.5:c.*1659_*1666delinsCTTATATT ENSP00000422424.1:n.*1659_*1666delinsCTTATATT
NM_006208.2:c.*44_*51delinsCTTATATT NP_006199.2:n.*44_*51delinsCTTATATT
XM_011535896.1:c.*44_*51delinsCTTATATT XP_011534198.1:n.*44_*51delinsCTTATATT
NM_006208.3:c.*44_*51delinsCTTATATT MANE Select NP_006199.2:n.*44_*51delinsCTTATATT