Canonical Allele Identifier: CA399047029

Gene: ZNF207

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.32366681C>A , CM000679.2:g.32366681C>A	GRCh38
NC_000017.10:g.30693700C>A , CM000679.1:g.30693700C>A	GRCh37
NC_000017.9:g.27717813C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394670.9:c.845C>A MANE Select	ENSP00000378165.4:p.Thr282Lys
ENST00000321233.10:c.797C>A	ENSP00000322777.6:p.Thr266Lys
ENST00000342555.10:c.854C>A	ENSP00000340029.6:p.Thr285Lys
ENST00000394670.8:c.845C>A	ENSP00000378165.4:p.Thr282Lys
ENST00000394673.6:c.829-1091C>A	ENSP00000378168.2:n.829-1091C>A
ENST00000577908.5:c.845C>A	ENSP00000464366.1:p.Thr282Lys
ENST00000581531.5:c.385C>A
ENST00000584696.1:n.5C>A
NM_001032293.2:c.829-1091C>A	NP_001027464.1:n.829-1091C>A
NM_001098507.1:c.845C>A	NP_001091977.1:p.Thr282Lys
NM_003457.3:c.797C>A	NP_003448.1:p.Thr266Lys
XM_005258029.1:c.806C>A	XP_005258086.1:p.Thr269Lys
XM_011525185.1:c.683C>A	XP_011523487.1:p.Thr228Lys
XR_934542.1:n.733C>A
XR_934543.1:n.733C>A
XR_934544.1:n.733C>A
XM_017025019.2:c.845C>A	XP_016880508.1:p.Thr282Lys
XR_001752611.2:n.974C>A
XR_001752612.2:n.974C>A
XR_001752613.2:n.931C>A
XR_001752614.2:n.926C>A
XR_001752615.2:n.935C>A
XR_001752616.2:n.967-1091C>A
XR_002958059.1:n.934C>A
XR_002958060.1:n.958-1091C>A
XR_002958061.1:n.919-1091C>A
XR_002958062.1:n.1040C>A
XR_002958063.1:n.1125C>A
XR_934542.3:n.974C>A
XR_934543.3:n.974C>A
NM_001032293.3:c.829-1091C>A	NP_001027464.1:n.829-1091C>A
NM_001098507.2:c.845C>A MANE Select	NP_001091977.1:p.Thr282Lys
NM_003457.4:c.797C>A	NP_003448.1:p.Thr266Lys