Canonical Allele Identifier: CA2838225267

Gene: ZNF341

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.33749087G>T , CM000682.2:g.33749087G>T	GRCh38
NC_000020.10:g.32336893G>T , CM000682.1:g.32336893G>T	GRCh37
NC_000020.9:g.31800554G>T	NCBI36
NG_053072.1:g.22328G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698694.1:c.489+15G>T	ENSP00000513875.1:n.489+15G>T
ENST00000375200.6:c.489+15G>T MANE Select	ENSP00000364346.1:n.489+15G>T
ENST00000342427.6:c.489+15G>T	ENSP00000344308.2:n.489+15G>T
ENST00000375200.5:c.489+15G>T	ENSP00000364346.1:n.489+15G>T
ENST00000483118.5:c.489+15G>T	ENSP00000432933.1:n.489+15G>T
ENST00000497876.5:c.*73+15G>T	ENSP00000434423.1:n.*73+15G>T
NM_001282933.1:c.489+15G>T	NP_001269862.1:n.489+15G>T
NM_001282935.1:c.219+15G>T	NP_001269864.1:n.219+15G>T
NM_032819.4:c.489+15G>T	NP_116208.3:n.489+15G>T
NR_104259.1:n.751+15G>T
XR_001754424.2:n.854+15G>T
XR_002958536.1:n.854+15G>T
NM_001282933.2:c.489+15G>T MANE Select	NP_001269862.1:n.489+15G>T
NM_001282935.2:c.219+15G>T	NP_001269864.1:n.219+15G>T
NM_032819.5:c.489+15G>T	NP_116208.3:n.489+15G>T
NR_104259.2:n.515+15G>T