Canonical Allele Identifier: CA407298748

Gene: ZNF417

Linked Data

• MyVariant Identifiers: chr19:g.58427752T>A (hg19) ; chr19:g.57916384T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57916384T>A , CM000681.2:g.57916384T>A	GRCh38
NC_000019.9:g.58427752T>A , CM000681.1:g.58427752T>A	GRCh37
NC_000019.8:g.63119564T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000312026.6:c.28A>T MANE Select	ENSP00000311319.4:p.Thr10Ser
ENST00000312026.5:c.28A>T	ENSP00000311319.4:p.Thr10Ser
ENST00000595559.1:c.28A>T	ENSP00000472272.1:p.Thr10Ser
ENST00000597515.5:c.-200A>T	ENSP00000471689.1:n.-200A>T
ENST00000598526.5:c.-203A>T	ENSP00000471325.1:n.-203A>T
ENST00000598629.5:c.-293A>T	ENSP00000471471.1:n.-293A>T
ENST00000599251.1:c.-296A>T	ENSP00000469176.1:n.-296A>T
ENST00000602124.1:c.-200A>T	ENSP00000470782.1:n.-200A>T
NM_001297734.1:c.28A>T	NP_001284663.1:p.Thr10Ser
NM_152475.2:c.28A>T	NP_689688.2:p.Thr10Ser
NM_152475.3:c.28A>T MANE Select	NP_689688.2:p.Thr10Ser
NM_001297734.2:c.28A>T	NP_001284663.1:p.Thr10Ser