Canonical Allele Identifier: CA365652238
Gene: ENPP1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.132198209A>G (hg19) chr6:g.131877069A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131877069A>G , CM000668.2:g.131877069A>G GRCh38
NC_000006.11:g.132198209A>G , CM000668.1:g.132198209A>G GRCh37
NC_000006.10:g.132239902A>G NCBI36
NG_008206.1:g.74054A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000683687.1:n.673A>G
ENST00000684536.1:n.299A>G
ENST00000647893.1:c.1801A>G MANE Select ENSP00000498074.1:p.Thr601Ala
ENST00000647981.1:n.486A>G
ENST00000650437.1:c.1292A>G
ENST00000360971.6:c.1801A>G ENSP00000354238.2:p.Thr601Ala
ENST00000459624.1:n.845A>G
ENST00000513998.5:c.*638A>G ENSP00000422424.1:n.*638A>G
NM_006208.2:c.1801A>G NP_006199.2:p.Thr601Ala
XM_011535896.1:c.691A>G XP_011534198.1:p.Thr231Ala
NM_006208.3:c.1801A>G MANE Select NP_006199.2:p.Thr601Ala
Search 100 bp 5'
Search 100 bp 3'