Canonical Allele Identifier: CA2259290820
Gene: ZPBP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39872249_39872253delinsATCTT , CM000679.2:g.39872249_39872253delinsATCTT GRCh38
NC_000017.10:g.38028502_38028506delinsATCTT , CM000679.1:g.38028502_38028506delinsATCTT GRCh37
NC_000017.9:g.35282028_35282032delinsATCTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000348931.9:c.407-21_407-17delinsATCTT MANE Select ENSP00000335384.5:n.407-21_407-17delinsATCTT
ENST00000348931.8:c.407-21_407-17delinsATCTT ENSP00000335384.5:n.407-21_407-17delinsATCTT
ENST00000377940.3:c.341-21_341-17delinsATCTT ENSP00000367174.3:n.341-21_341-17delinsATCTT
ENST00000583811.5:c.53-21_53-17delinsATCTT ENSP00000462463.1:n.53-21_53-17delinsATCTT
ENST00000584588.5:c.406+624_406+628delinsATCTT ENSP00000462067.1:n.406+624_406+628delinsATCTT
NM_198844.2:c.341-21_341-17delinsATCTT NP_942141.2:n.341-21_341-17delinsATCTT
NM_199321.2:c.407-21_407-17delinsATCTT NP_955353.1:n.407-21_407-17delinsATCTT
XM_011524298.1:c.407-21_407-17delinsATCTT XP_011522600.1:n.407-21_407-17delinsATCTT
XR_002957959.1:n.598-21_598-17delinsATCTT
NM_198844.3:c.341-21_341-17delinsATCTT NP_942141.2:n.341-21_341-17delinsATCTT
NM_199321.3:c.407-21_407-17delinsATCTT MANE Select NP_955353.1:n.407-21_407-17delinsATCTT