Canonical Allele Identifier: CA9819081

Gene: ZNF341

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33745085C>A , CM000682.2:g.33745085C>A	GRCh38
NC_000020.10:g.32332891C>A , CM000682.1:g.32332891C>A	GRCh37
NC_000020.9:g.31796552C>A	NCBI36
NG_053072.1:g.18326C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001282933.2:c.143-18C>A MANE Select	NP_001269862.1:n.143-18C>A
ENST00000375200.6:c.143-18C>A MANE Select	ENSP00000364346.1:n.143-18C>A
NM_001282933.1:c.143-18C>A	NP_001269862.1:n.143-18C>A
NM_001282935.1:c.70-3838C>A	NP_001269864.1:n.70-3838C>A
NM_001282935.2:c.70-3838C>A	NP_001269864.1:n.70-3838C>A
NM_032819.4:c.143-18C>A	NP_116208.3:n.143-18C>A
NM_032819.5:c.143-18C>A	NP_116208.3:n.143-18C>A
NR_104259.1:n.405-18C>A
NR_104259.2:n.169-18C>A
ENST00000342427.6:c.143-18C>A	ENSP00000344308.2:n.143-18C>A
ENST00000375200.5:c.143-18C>A	ENSP00000364346.1:n.143-18C>A
ENST00000483118.5:c.143-18C>A	ENSP00000432933.1:n.143-18C>A
ENST00000497876.5:c.143-3838C>A	ENSP00000434423.1:n.143-3838C>A
ENST00000698694.1:c.143-18C>A	ENSP00000513875.1:n.143-18C>A
XR_001754424.2:n.508-18C>A
XR_002958536.1:n.508-18C>A