Canonical Allele Identifier: CA819051336

Gene: ENPP3

Linked Data

• dbSNP Id: rs1468814115
• MyVariant Identifiers: chr6:g.132058871G>A (hg19) ; chr6:g.131737731G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131737731G>A , CM000668.2:g.131737731G>A	GRCh38
NC_000006.11:g.132058871G>A , CM000668.1:g.132058871G>A	GRCh37
NC_000006.10:g.132100564G>A	NCBI36
NG_033982.1:g.105430G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000357639.8:c.2168-300G>A MANE Select	ENSP00000350265.3:n.2168-300G>A
ENST00000357639.7:c.2168-300G>A	ENSP00000350265.3:n.2168-300G>A
ENST00000358229.6:c.*40-300G>A	ENSP00000350964.5:n.*40-300G>A
ENST00000414305.5:c.2168-300G>A	ENSP00000406261.1:n.2168-300G>A
NM_005021.3:c.2168-300G>A	NP_005012.2:n.2168-300G>A
NM_005021.4:c.2168-300G>A	NP_005012.2:n.2168-300G>A
NR_133007.1:n.2182-300G>A
XM_011535897.1:c.1406-300G>A	XP_011534199.1:n.1406-300G>A
XM_017010932.1:c.1937-300G>A	XP_016866421.1:n.1937-300G>A
XR_001743464.2:n.2366-300G>A
NM_005021.5:c.2168-300G>A MANE Select	NP_005012.2:n.2168-300G>A
NR_133007.2:n.2115-300G>A