Canonical Allele Identifier: CA2680371796
Gene: ENPP1 HGNC NCBI

Linked Data

gnomAD v4: 6-131890612-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890612A>T , CM000668.2:g.131890612A>T GRCh38
NC_000006.11:g.132211752A>T , CM000668.1:g.132211752A>T GRCh37
NC_000006.10:g.132253445A>T NCBI36
NG_008206.1:g.87597A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1310A>T
ENST00000647893.1:c.*101A>T MANE Select ENSP00000498074.1:n.*101A>T
ENST00000360971.6:c.*101A>T ENSP00000354238.2:n.*101A>T
ENST00000513998.5:c.*1716A>T ENSP00000422424.1:n.*1716A>T
NM_006208.2:c.*101A>T NP_006199.2:n.*101A>T
XM_011535896.1:c.*101A>T XP_011534198.1:n.*101A>T
NM_006208.3:c.*101A>T MANE Select NP_006199.2:n.*101A>T
Search 100 bp 5'
Search 100 bp 3'