Canonical Allele Identifier: CA4553206

Gene: ZNF746

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.149494455T>C , CM000669.2:g.149494455T>C	GRCh38
NC_000007.13:g.149191546T>C , CM000669.1:g.149191546T>C	GRCh37
NC_000007.12:g.148822479T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001394198.1:c.73A>G MANE Select	NP_001381127.1:p.Ile25Val
ENST00000458143.7:c.73A>G MANE Select	ENSP00000395007.3:p.Ile25Val
NM_001163474.1:c.73A>G	NP_001156946.1:p.Ile25Val
NM_001163474.2:c.73A>G	NP_001156946.1:p.Ile25Val
NM_001363517.1:c.73A>G	NP_001350446.1:p.Ile25Val
NM_001363517.2:c.73A>G	NP_001350446.1:p.Ile25Val
NM_152557.4:c.73A>G	NP_689770.3:p.Ile25Val
NM_152557.5:c.73A>G	NP_689770.3:p.Ile25Val
ENST00000340622.7:c.73A>G	ENSP00000345140.3:p.Ile25Val
ENST00000340622.8:c.73A>G	ENSP00000345140.3:p.Ile25Val
ENST00000458143.6:c.73A>G	ENSP00000395007.2:p.Ile25Val
ENST00000461958.2:c.73A>G	ENSP00000420329.2:p.Ile25Val
ENST00000644635.1:c.73A>G	ENSP00000493970.1:p.Ile25Val
ENST00000685153.1:c.73A>G	ENSP00000508891.1:p.Ile25Val
XM_005249955.1:c.73A>G	XP_005250012.1:p.Ile25Val
XM_005249955.2:c.73A>G	XP_005250012.1:p.Ile25Val
XM_005249956.1:c.73A>G	XP_005250013.1:p.Ile25Val
XM_005249957.1:c.34A>G	XP_005250014.1:p.Ile12Val
XM_011515838.1:c.34A>G	XP_011514140.1:p.Ile12Val