Canonical Allele Identifier: CA2838206381

Gene: ZNF341

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33745395A>T , CM000682.2:g.33745395A>T	GRCh38
NC_000020.10:g.32333201A>T , CM000682.1:g.32333201A>T	GRCh37
NC_000020.9:g.31796862A>T	NCBI36
NG_053072.1:g.18636A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698694.1:c.339+96A>T	ENSP00000513875.1:n.339+96A>T
ENST00000375200.6:c.339+96A>T MANE Select	ENSP00000364346.1:n.339+96A>T
ENST00000342427.6:c.339+96A>T	ENSP00000344308.2:n.339+96A>T
ENST00000375200.5:c.339+96A>T	ENSP00000364346.1:n.339+96A>T
ENST00000483118.5:c.339+96A>T	ENSP00000432933.1:n.339+96A>T
ENST00000497876.5:c.143-3528A>T	ENSP00000434423.1:n.143-3528A>T
NM_001282933.1:c.339+96A>T	NP_001269862.1:n.339+96A>T
NM_001282935.1:c.70-3528A>T	NP_001269864.1:n.70-3528A>T
NM_032819.4:c.339+96A>T	NP_116208.3:n.339+96A>T
NR_104259.1:n.601+96A>T
XR_001754424.2:n.704+96A>T
XR_002958536.1:n.704+96A>T
NM_001282933.2:c.339+96A>T MANE Select	NP_001269862.1:n.339+96A>T
NM_001282935.2:c.70-3528A>T	NP_001269864.1:n.70-3528A>T
NM_032819.5:c.339+96A>T	NP_116208.3:n.339+96A>T
NR_104259.2:n.365+96A>T