Canonical Allele Identifier: CA507756820

Gene: ZNF224

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44095462C>A , CM000681.2:g.44095462C>A	GRCh38
NC_000019.9:g.44599615C>A , CM000681.1:g.44599615C>A	GRCh37
NC_000019.8:g.49291455C>A	NCBI36
NG_051221.1:g.6134C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000684943.1:c.-69+932C>A	ENSP00000509045.1:n.-69+932C>A
ENST00000693561.1:c.-157-881C>A MANE Select	ENSP00000508532.1:n.-157-881C>A
ENST00000336976.10:c.-157-881C>A	ENSP00000337368.5:n.-157-881C>A
ENST00000586978.1:n.374+304C>A
ENST00000589060.1:n.1073C>A
ENST00000589680.5:c.-157-881C>A	ENSP00000465000.1:n.-157-881C>A
ENST00000590614.5:n.103-881C>A
NM_013398.2:c.-157-881C>A	NP_037530.2:n.-157-881C>A
XM_005259221.2:c.-157-881C>A	XP_005259278.1:n.-157-881C>A
NM_001321645.1:c.-157-881C>A	NP_001308574.1:n.-157-881C>A
NM_013398.3:c.-157-881C>A	NP_037530.2:n.-157-881C>A
XM_017027261.2:c.-1038C>A	XP_016882750.1:n.-1038C>A
NM_001321645.2:c.-157-881C>A	NP_001308574.1:n.-157-881C>A
NM_013398.4:c.-157-881C>A	NP_037530.2:n.-157-881C>A
NM_001321645.3:c.-157-881C>A MANE Select	NP_001308574.1:n.-157-881C>A
NM_013398.5:c.-157-881C>A	NP_037530.2:n.-157-881C>A