Canonical Allele Identifier: CA408654373

Gene: ZNF341

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33761887T>C , CM000682.2:g.33761887T>C	GRCh38
NC_000020.10:g.32349693T>C , CM000682.1:g.32349693T>C	GRCh37
NC_000020.9:g.31813354T>C	NCBI36
NG_053072.1:g.35128T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698694.1:c.489+12815T>C	ENSP00000513875.1:n.489+12815T>C
ENST00000698695.1:c.456+3081T>C	ENSP00000513876.1:n.456+3081T>C
ENST00000375200.6:c.1054T>C MANE Select	ENSP00000364346.1:p.Cys352Arg
ENST00000342427.6:c.1033T>C	ENSP00000344308.2:p.Cys345Arg
ENST00000375200.5:c.1054T>C	ENSP00000364346.1:p.Cys352Arg
ENST00000483118.5:c.1054T>C	ENSP00000432933.1:p.Cys352Arg
ENST00000497876.5:c.*638T>C	ENSP00000434423.1:n.*638T>C
NM_001282933.1:c.1054T>C	NP_001269862.1:p.Cys352Arg
NM_001282935.1:c.784T>C	NP_001269864.1:p.Cys262Arg
NM_032819.4:c.1033T>C	NP_116208.3:p.Cys345Arg
NR_104259.1:n.1316T>C
XR_001754424.2:n.1419T>C
XR_002958536.1:n.1398T>C
NM_001282933.2:c.1054T>C MANE Select	NP_001269862.1:p.Cys352Arg
NM_001282935.2:c.784T>C	NP_001269864.1:p.Cys262Arg
NM_032819.5:c.1033T>C	NP_116208.3:p.Cys345Arg
NR_104259.2:n.1080T>C