Canonical Allele Identifier: CA774959437

Gene: ZBTB4

Linked Data

• dbSNP Id: rs1312773635
• gnomAD v3: 17-7459576-GA-G
• gnomAD v4: 17-7459576-GA-G
• MyVariant Identifiers: chr17:g.7362896del (hg19) ; chr17:g.7459577del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.7459579del , CM000679.2:g.7459579del	GRCh38
NC_000017.10:g.7362898del , CM000679.1:g.7362898del	GRCh37
NC_000017.9:g.7303622del	NCBI36
NG_008026.1:g.19493del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380599.9:c.*2363del MANE Select	ENSP00000369973.4:n.*2363del
ENST00000311403.4:c.*2363del	ENSP00000307858.4:n.*2363del
ENST00000380599.8:c.*2363del	ENSP00000369973.4:n.*2363del
NM_001128833.1:c.*2362del	NP_001122305.1:n.*2362del
NM_020899.3:c.*2362del	NP_065950.2:n.*2362del
XM_006721563.2:c.*2363del	XP_006721626.1:n.*2363del
XM_006721564.1:c.*2363del	XP_006721627.1:n.*2363del
XM_011523972.1:c.*2363del	XP_011522274.1:n.*2363del
XM_006721563.3:c.*2363del	XP_006721626.1:n.*2363del
XM_006721564.2:c.*2363del	XP_006721627.1:n.*2363del
XM_011523972.2:c.*2363del	XP_011522274.1:n.*2363del
NM_001128833.2:c.*2363del MANE Select	NP_001122305.1:n.*2363del
NM_020899.4:c.*2363del	NP_065950.2:n.*2363del