Canonical Allele Identifier: CA347313210

Gene: TET3

Linked Data - Predicted Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74093667G>A , CM000664.2:g.74093667G>A	GRCh38
NC_000002.11:g.74320794G>A , CM000664.1:g.74320794G>A	GRCh37
NC_000002.10:g.74174302G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409262.8:c.3267+1G>A MANE Select	ENSP00000386869.3:n.3267+1G>A
ENST00000305799.8:c.2988+1G>A	ENSP00000307803.8:n.2988+1G>A
ENST00000409262.7:c.3267+1G>A	ENSP00000386869.3:n.3267+1G>A
NM_001287491.1:c.3267+1G>A	NP_001274420.1:n.3267+1G>A
XM_005264187.2:c.3267+1G>A	XP_005264244.1:n.3267+1G>A
XM_011532682.1:c.3315+1G>A	XP_011530984.1:n.3315+1G>A
XM_011532683.1:c.3315+1G>A	XP_011530985.1:n.3315+1G>A
XM_011532684.1:c.3315+1G>A	XP_011530986.1:n.3315+1G>A
XM_011532685.1:c.3258+1G>A	XP_011530987.1:n.3258+1G>A
XM_011532686.1:c.3210+1G>A	XP_011530988.1:n.3210+1G>A
XM_011532687.1:c.3036+1G>A	XP_011530989.1:n.3036+1G>A
XM_011532689.1:c.741+1G>A	XP_011530991.1:n.741+1G>A
XM_011532690.1:c.741+1G>A	XP_011530992.1:n.741+1G>A
NM_001287491.2:c.3267+1G>A MANE Select	NP_001274420.1:n.3267+1G>A
NM_001366022.1:c.2988+1G>A	NP_001352951.1:n.2988+1G>A
XM_011532682.2:c.3315+1G>A	XP_011530984.1:n.3315+1G>A
XM_011532683.2:c.3315+1G>A	XP_011530985.1:n.3315+1G>A
XM_011532684.2:c.3315+1G>A	XP_011530986.1:n.3315+1G>A
XM_011532685.2:c.3258+1G>A	XP_011530987.1:n.3258+1G>A
XM_011532686.2:c.3210+1G>A	XP_011530988.1:n.3210+1G>A
XM_011532687.2:c.3036+1G>A	XP_011530989.1:n.3036+1G>A
XM_017003566.1:c.3315+1G>A	XP_016859055.1:n.3315+1G>A
XM_024452745.1:c.3315+1G>A	XP_024308513.1:n.3315+1G>A
XM_024452746.1:c.3267+1G>A	XP_024308514.1:n.3267+1G>A
XM_024452747.1:c.741+1G>A	XP_024308515.1:n.741+1G>A