Canonical Allele Identifier: CA365651814
Gene: ENPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131877005G>T , CM000668.2:g.131877005G>T GRCh38
NC_000006.11:g.132198145G>T , CM000668.1:g.132198145G>T GRCh37
NC_000006.10:g.132239838G>T NCBI36
NG_008206.1:g.73990G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000683687.1:n.609G>T
ENST00000684536.1:n.235G>T
ENST00000647893.1:c.1737G>T MANE Select ENSP00000498074.1:p.Leu579Phe
ENST00000647981.1:n.422G>T
ENST00000650437.1:c.1228G>T
ENST00000360971.6:c.1737G>T ENSP00000354238.2:p.Leu579Phe
ENST00000459624.1:n.781G>T
ENST00000513998.5:c.*574G>T ENSP00000422424.1:n.*574G>T
NM_006208.2:c.1737G>T NP_006199.2:p.Leu579Phe
XM_011535896.1:c.627G>T XP_011534198.1:p.Leu209Phe
NM_006208.3:c.1737G>T MANE Select NP_006199.2:p.Leu579Phe