Canonical Allele Identifier: CA499931613

Gene: ZPBP2

Linked Data

• MyVariant Identifiers: chr17:g.38028566T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872313T>C , CM000679.2:g.39872313T>C	GRCh38
NC_000017.10:g.38028566T>C , CM000679.1:g.38028566T>C	GRCh37
NC_000017.9:g.35282092T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.450T>C MANE Select	ENSP00000335384.5:p.Phe150=
ENST00000348931.8:c.450T>C	ENSP00000335384.5:p.Phe150=
ENST00000377940.3:c.384T>C	ENSP00000367174.3:p.Phe128=
ENST00000583811.5:c.96T>C	ENSP00000462463.1:p.Phe32=
ENST00000584588.5:c.406+688T>C	ENSP00000462067.1:n.406+688T>C
NM_198844.2:c.384T>C	NP_942141.2:p.Phe128=
NM_199321.2:c.450T>C	NP_955353.1:p.Phe150=
XM_011524298.1:c.450T>C	XP_011522600.1:p.Phe150=
XR_002957959.1:n.641T>C
NM_198844.3:c.384T>C	NP_942141.2:p.Phe128=
NM_199321.3:c.450T>C MANE Select	NP_955353.1:p.Phe150=