Canonical Allele Identifier: CA1664228259
Gene: ENPP3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131737708_131737709delinsTC , CM000668.2:g.131737708_131737709delinsTC GRCh38
NC_000006.11:g.132058848_132058849delinsTC , CM000668.1:g.132058848_132058849delinsTC GRCh37
NC_000006.10:g.132100541_132100542delinsTC NCBI36
NG_033982.1:g.105407_105408delinsTC

Transcript Alleles

HGVS Amino-acid change
ENST00000357639.8:c.2167+276_2167+277delinsTC MANE Select ENSP00000350265.3:n.2167+276_2167+277deli...
ENST00000357639.7:c.2167+276_2167+277delinsTC ENSP00000350265.3:n.2167+276_2167+277deli...
ENST00000358229.6:c.*39+276_*39+277delinsTC ENSP00000350964.5:n.*39+276_*39+277delins...
ENST00000414305.5:c.2167+276_2167+277delinsTC ENSP00000406261.1:n.2167+276_2167+277deli...
NM_005021.3:c.2167+276_2167+277delinsTC NP_005012.2:n.2167+276_2167+277delinsTC
NM_005021.4:c.2167+276_2167+277delinsTC NP_005012.2:n.2167+276_2167+277delinsTC
NR_133007.1:n.2181+276_2181+277delinsTC
XM_011535897.1:c.1405+276_1405+277delinsTC XP_011534199.1:n.1405+276_1405+277delinsT...
XM_017010932.1:c.1936+276_1936+277delinsTC XP_016866421.1:n.1936+276_1936+277delinsT...
XR_001743464.2:n.2365+276_2365+277delinsTC
NM_005021.5:c.2167+276_2167+277delinsTC MANE Select NP_005012.2:n.2167+276_2167+277delinsTC
NR_133007.2:n.2114+276_2114+277delinsTC