Canonical Allele Identifier: CA2680371734
Gene: ENPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890314T>G , CM000668.2:g.131890314T>G GRCh38
NC_000006.11:g.132211454T>G , CM000668.1:g.132211454T>G GRCh37
NC_000006.10:g.132253147T>G NCBI36
NG_008206.1:g.87299T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684674.1:n.1039-27T>G
ENST00000647893.1:c.2608-27T>G MANE Select ENSP00000498074.1:n.2608-27T>G
ENST00000360971.6:c.2608-27T>G ENSP00000354238.2:n.2608-27T>G
ENST00000513998.5:c.*1445-27T>G ENSP00000422424.1:n.*1445-27T>G
NM_006208.2:c.2608-27T>G NP_006199.2:n.2608-27T>G
XM_011535896.1:c.1498-27T>G XP_011534198.1:n.1498-27T>G
NM_006208.3:c.2608-27T>G MANE Select NP_006199.2:n.2608-27T>G