Canonical Allele Identifier: CA1664283082
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890311_131890316delinsACTTTT , CM000668.2:g.131890311_131890316delinsACTTTT GRCh38
NC_000006.11:g.132211451_132211456delinsACTTTT , CM000668.1:g.132211451_132211456delinsACTTTT GRCh37
NC_000006.10:g.132253144_132253149delinsACTTTT NCBI36
NG_008206.1:g.87296_87301delinsACTTTT

Transcript Alleles

HGVS Amino-acid change
ENST00000684674.1:n.1039-30_1039-25delinsACTTTT
ENST00000647893.1:c.2608-30_2608-25delinsACTTTT MANE Select ENSP00000498074.1:n.2608-30_2608-25delins...
ENST00000360971.6:c.2608-30_2608-25delinsACTTTT ENSP00000354238.2:n.2608-30_2608-25delins...
ENST00000513998.5:c.*1445-30_*1445-25delinsACTTTT ENSP00000422424.1:n.*1445-30_*1445-25deli...
NM_006208.2:c.2608-30_2608-25delinsACTTTT NP_006199.2:n.2608-30_2608-25delinsACTTTT...
XM_011535896.1:c.1498-30_1498-25delinsACTTTT XP_011534198.1:n.1498-30_1498-25delinsACT...
NM_006208.3:c.2608-30_2608-25delinsACTTTT MANE Select NP_006199.2:n.2608-30_2608-25delinsACTTTT...