Canonical Allele Identifier: CA50414918

Gene: TET3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.73986482G>A , CM000664.2:g.73986482G>A	GRCh38
NC_000002.11:g.74213609G>A , CM000664.1:g.74213609G>A	GRCh37
NC_000002.10:g.74067117G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409262.8:c.79G>A MANE Select	ENSP00000386869.3:p.Val27Ile
ENST00000409262.7:c.79G>A	ENSP00000386869.3:p.Val27Ile
NM_001287491.1:c.79G>A	NP_001274420.1:p.Val27Ile
XM_005264187.2:c.79G>A	XP_005264244.1:p.Val27Ile
XM_011532682.1:c.79G>A	XP_011530984.1:p.Val27Ile
XM_011532683.1:c.79G>A	XP_011530985.1:p.Val27Ile
XM_011532684.1:c.79G>A	XP_011530986.1:p.Val27Ile
XM_011532685.1:c.79G>A	XP_011530987.1:p.Val27Ile
XM_011532686.1:c.79G>A	XP_011530988.1:p.Val27Ile
XM_011532688.1:c.79G>A	XP_011530990.1:p.Val27Ile
NM_001287491.2:c.79G>A MANE Select	NP_001274420.1:p.Val27Ile
XM_011532682.2:c.79G>A	XP_011530984.1:p.Val27Ile
XM_011532683.2:c.79G>A	XP_011530985.1:p.Val27Ile
XM_011532684.2:c.79G>A	XP_011530986.1:p.Val27Ile
XM_011532685.2:c.79G>A	XP_011530987.1:p.Val27Ile
XM_011532686.2:c.79G>A	XP_011530988.1:p.Val27Ile
XM_011532688.2:c.79G>A	XP_011530990.1:p.Val27Ile
XM_017003566.1:c.79G>A	XP_016859055.1:p.Val27Ile
XM_024452745.1:c.79G>A	XP_024308513.1:p.Val27Ile
XM_024452746.1:c.79G>A	XP_024308514.1:p.Val27Ile