Canonical Allele Identifier: CA719892119

Gene: ZNF668

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.31071754A>T , CM000678.2:g.31071754A>T	GRCh38
NC_000016.9:g.31083075A>T , CM000678.1:g.31083075A>T	GRCh37
NC_000016.8:g.30990576A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300849.5:c.-23+1905T>A MANE Select	ENSP00000300849.4:n.-23+1905T>A
ENST00000300849.4:c.-23+1905T>A	ENSP00000300849.4:n.-23+1905T>A
ENST00000394983.6:c.-23+1132T>A	ENSP00000378434.2:n.-23+1132T>A
ENST00000414399.1:c.-23+1905T>A	ENSP00000412340.1:n.-23+1905T>A
ENST00000417935.1:c.-23+986T>A	ENSP00000390671.1:n.-23+986T>A
ENST00000538906.5:c.-23+986T>A	ENSP00000440149.1:n.-23+986T>A
ENST00000564456.1:n.526+1905T>A
NM_001172668.1:c.-23+986T>A	NP_001166139.1:n.-23+986T>A
NM_024706.4:c.-23+1905T>A	NP_078982.3:n.-23+1905T>A
XM_011545949.1:c.-68+1905T>A	XP_011544251.1:n.-68+1905T>A
NM_024706.5:c.-23+1905T>A MANE Select	NP_078982.3:n.-23+1905T>A
NM_001172668.2:c.-23+986T>A	NP_001166139.1:n.-23+986T>A