Canonical Allele Identifier: CA365660996
Gene: ENPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890455G>T , CM000668.2:g.131890455G>T GRCh38
NC_000006.11:g.132211595G>T , CM000668.1:g.132211595G>T GRCh37
NC_000006.10:g.132253288G>T NCBI36
NG_008206.1:g.87440G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1153G>T
ENST00000647893.1:c.2722G>T MANE Select ENSP00000498074.1:p.Val908Phe
ENST00000360971.6:c.2722G>T ENSP00000354238.2:p.Val908Phe
ENST00000513998.5:c.*1559G>T ENSP00000422424.1:n.*1559G>T
NM_006208.2:c.2722G>T NP_006199.2:p.Val908Phe
XM_011535896.1:c.1612G>T XP_011534198.1:p.Val538Phe
NM_006208.3:c.2722G>T MANE Select NP_006199.2:p.Val908Phe