Canonical Allele Identifier: CA499931615

Gene: ZPBP2

Linked Data

• MyVariant Identifiers: chr17:g.38028569C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872316C>G , CM000679.2:g.39872316C>G	GRCh38
NC_000017.10:g.38028569C>G , CM000679.1:g.38028569C>G	GRCh37
NC_000017.9:g.35282095C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.453C>G MANE Select	ENSP00000335384.5:p.Thr151=
ENST00000348931.8:c.453C>G	ENSP00000335384.5:p.Thr151=
ENST00000377940.3:c.387C>G	ENSP00000367174.3:p.Thr129=
ENST00000583811.5:c.99C>G	ENSP00000462463.1:p.Thr33=
ENST00000584588.5:c.406+691C>G	ENSP00000462067.1:n.406+691C>G
NM_198844.2:c.387C>G	NP_942141.2:p.Thr129=
NM_199321.2:c.453C>G	NP_955353.1:p.Thr151=
XM_011524298.1:c.453C>G	XP_011522600.1:p.Thr151=
XR_002957959.1:n.644C>G
NM_198844.3:c.387C>G	NP_942141.2:p.Thr129=
NM_199321.3:c.453C>G MANE Select	NP_955353.1:p.Thr151=