Canonical Allele Identifier: CA291452116

Gene: ZNF652

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.49359387G>A , CM000679.2:g.49359387G>A	GRCh38
NC_000017.10:g.47436749G>A , CM000679.1:g.47436749G>A	GRCh37
NC_000017.9:g.44791748G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000430262.3:c.-259+2522C>T MANE Select	ENSP00000416305.2:n.-259+2522C>T
ENST00000362063.6:c.-259+3026C>T	ENSP00000354686.2:n.-259+3026C>T
ENST00000430262.2:c.-259+2522C>T	ENSP00000416305.2:n.-259+2522C>T
ENST00000508237.5:c.-383+2522C>T	ENSP00000424848.1:n.-383+2522C>T
NM_001145365.1:c.-259+2522C>T	NP_001138837.1:n.-259+2522C>T
NM_014897.2:c.-259+3026C>T	NP_055712.1:n.-259+3026C>T
NR_135579.1:n.206+2522C>T
XM_024450654.1:c.-383+2522C>T	XP_024306422.1:n.-383+2522C>T
NM_001145365.2:c.-259+2522C>T	NP_001138837.1:n.-259+2522C>T
NR_135579.2:n.342+2522C>T
NM_001145365.3:c.-259+2522C>T MANE Select	NP_001138837.1:n.-259+2522C>T