Canonical Allele Identifier: CA347319497

Gene: TET3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74101122C>A , CM000664.2:g.74101122C>A	GRCh38
NC_000002.11:g.74328249C>A , CM000664.1:g.74328249C>A	GRCh37
NC_000002.10:g.74181757C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409262.8:c.4334C>A MANE Select	ENSP00000386869.3:p.Ser1445Tyr
ENST00000305799.8:c.4055C>A	ENSP00000307803.8:p.Ser1352Tyr
ENST00000409262.7:c.4334C>A	ENSP00000386869.3:p.Ser1445Tyr
NM_001287491.1:c.4334C>A	NP_001274420.1:p.Ser1445Tyr
XM_005264187.2:c.4334C>A	XP_005264244.1:p.Ser1445Tyr
XM_011532682.1:c.4382C>A	XP_011530984.1:p.Ser1461Tyr
XM_011532683.1:c.4382C>A	XP_011530985.1:p.Ser1461Tyr
XM_011532684.1:c.4382C>A	XP_011530986.1:p.Ser1461Tyr
XM_011532685.1:c.4325C>A	XP_011530987.1:p.Ser1442Tyr
XM_011532686.1:c.4277C>A	XP_011530988.1:p.Ser1426Tyr
XM_011532687.1:c.4103C>A	XP_011530989.1:p.Ser1368Tyr
XM_011532689.1:c.1808C>A	XP_011530991.1:p.Ser603Tyr
XM_011532690.1:c.1808C>A	XP_011530992.1:p.Ser603Tyr
NM_001287491.2:c.4334C>A MANE Select	NP_001274420.1:p.Ser1445Tyr
NM_001366022.1:c.4055C>A	NP_001352951.1:p.Ser1352Tyr
XM_011532682.2:c.4382C>A	XP_011530984.1:p.Ser1461Tyr
XM_011532683.2:c.4382C>A	XP_011530985.1:p.Ser1461Tyr
XM_011532684.2:c.4382C>A	XP_011530986.1:p.Ser1461Tyr
XM_011532685.2:c.4325C>A	XP_011530987.1:p.Ser1442Tyr
XM_011532686.2:c.4277C>A	XP_011530988.1:p.Ser1426Tyr
XM_011532687.2:c.4103C>A	XP_011530989.1:p.Ser1368Tyr
XM_017003566.1:c.4382C>A	XP_016859055.1:p.Ser1461Tyr
XM_024452745.1:c.3315+7456C>A	XP_024308513.1:n.3315+7456C>A
XM_024452746.1:c.3267+7456C>A	XP_024308514.1:n.3267+7456C>A
XM_024452747.1:c.1808C>A	XP_024308515.1:p.Ser603Tyr