Canonical Allele Identifier: CA15432498

Gene: ZNF292

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.87157345T>C , CM000668.2:g.87157345T>C	GRCh38
NC_000006.11:g.87867063T>C , CM000668.1:g.87867063T>C	GRCh37
NC_000006.10:g.87923782T>C	NCBI36
NG_054887.1:g.6795T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392985.4:c.168+1586T>C	ENSP00000430569.1:n.168+1586T>C
ENST00000466062.3:c.116+1586T>C
ENST00000699914.1:c.168+1586T>C	ENSP00000514683.1:n.168+1586T>C
ENST00000699923.1:c.165+1984T>C	ENSP00000514690.1:n.165+1984T>C
ENST00000699924.1:n.191+1586T>C
ENST00000699925.1:c.168+1586T>C	ENSP00000514691.1:n.168+1586T>C
ENST00000699990.1:n.167+1586T>C
ENST00000369577.8:c.168+1586T>C MANE Select	ENSP00000358590.3:n.168+1586T>C
ENST00000339907.8:c.168+1586T>C	ENSP00000342847.4:n.168+1586T>C
ENST00000369577.7:c.168+1586T>C	ENSP00000358590.3:n.168+1586T>C
ENST00000369578.6:n.195+1586T>C
ENST00000392985.3:c.168+1586T>C	ENSP00000430569.1:n.168+1586T>C
ENST00000496806.2:c.139+1586T>C	ENSP00000428857.1:n.139+1586T>C
ENST00000518845.1:c.168+1586T>C	ENSP00000428925.1:n.168+1586T>C
NM_015021.1:c.168+1586T>C	NP_055836.1:n.168+1586T>C
XM_011535625.1:c.-657+1586T>C	XP_011533927.1:n.-657+1586T>C
NM_001351444.1:c.-398+1586T>C	NP_001338373.1:n.-398+1586T>C
NM_015021.2:c.168+1586T>C	NP_055836.1:n.168+1586T>C
XM_011535625.2:c.-657+1586T>C	XP_011533927.1:n.-657+1586T>C
NM_015021.3:c.168+1586T>C MANE Select	NP_055836.1:n.168+1586T>C
NM_001351444.2:c.-398+1586T>C	NP_001338373.1:n.-398+1586T>C