Canonical Allele Identifier: CA2259290743

Gene: ZPBP2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39872046_39872049delinsCTTG , CM000679.2:g.39872046_39872049delinsCTTG	GRCh38
NC_000017.10:g.38028299_38028302delinsCTTG , CM000679.1:g.38028299_38028302delinsCTTG	GRCh37
NC_000017.9:g.35281825_35281828delinsCTTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000348931.9:c.407-224_407-221delinsCTTG MANE Select	ENSP00000335384.5:n.407-224_407-221delinsCTTG
ENST00000348931.8:c.407-224_407-221delinsCTTG	ENSP00000335384.5:n.407-224_407-221delinsCTTG
ENST00000377940.3:c.341-224_341-221delinsCTTG	ENSP00000367174.3:n.341-224_341-221delinsCTTG
ENST00000583811.5:c.53-224_53-221delinsCTTG	ENSP00000462463.1:n.53-224_53-221delinsCTTG
ENST00000584588.5:c.406+421_406+424delinsCTTG	ENSP00000462067.1:n.406+421_406+424delinsCTTG
NM_198844.2:c.341-224_341-221delinsCTTG	NP_942141.2:n.341-224_341-221delinsCTTG
NM_199321.2:c.407-224_407-221delinsCTTG	NP_955353.1:n.407-224_407-221delinsCTTG
XM_011524298.1:c.407-224_407-221delinsCTTG	XP_011522600.1:n.407-224_407-221delinsCTTG
XR_002957959.1:n.598-224_598-221delinsCTTG
NM_198844.3:c.341-224_341-221delinsCTTG	NP_942141.2:n.341-224_341-221delinsCTTG
NM_199321.3:c.407-224_407-221delinsCTTG MANE Select	NP_955353.1:n.407-224_407-221delinsCTTG