Canonical Allele Identifier: CA1718696

Gene: TET3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.74047775C>G , CM000664.2:g.74047775C>G	GRCh38
NC_000002.11:g.74274902C>G , CM000664.1:g.74274902C>G	GRCh37
NC_000002.10:g.74128410C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001287491.2:c.1858C>G MANE Select	NP_001274420.1:p.Leu620Val
ENST00000409262.8:c.1858C>G MANE Select	ENSP00000386869.3:p.Leu620Val
NM_001287491.1:c.1858C>G	NP_001274420.1:p.Leu620Val
NM_001366022.1:c.1579C>G	NP_001352951.1:p.Leu527Val
ENST00000305799.8:c.1579C>G	ENSP00000307803.8:p.Leu527Val
ENST00000409262.7:c.1858C>G	ENSP00000386869.3:p.Leu620Val
ENST00000475405.2:n.616C>G
XM_005264187.2:c.1858C>G	XP_005264244.1:p.Leu620Val
XM_011532682.1:c.1858C>G	XP_011530984.1:p.Leu620Val
XM_011532682.2:c.1858C>G	XP_011530984.1:p.Leu620Val
XM_011532683.1:c.1858C>G	XP_011530985.1:p.Leu620Val
XM_011532683.2:c.1858C>G	XP_011530985.1:p.Leu620Val
XM_011532684.1:c.1858C>G	XP_011530986.1:p.Leu620Val
XM_011532684.2:c.1858C>G	XP_011530986.1:p.Leu620Val
XM_011532685.1:c.1801C>G	XP_011530987.1:p.Leu601Val
XM_011532685.2:c.1801C>G	XP_011530987.1:p.Leu601Val
XM_011532686.1:c.1801C>G	XP_011530988.1:p.Leu601Val
XM_011532686.2:c.1801C>G	XP_011530988.1:p.Leu601Val
XM_011532687.1:c.1579C>G	XP_011530989.1:p.Leu527Val
XM_011532687.2:c.1579C>G	XP_011530989.1:p.Leu527Val
XM_011532688.1:c.1858C>G	XP_011530990.1:p.Leu620Val
XM_011532688.2:c.1858C>G	XP_011530990.1:p.Leu620Val
XM_011532689.1:c.-80-25774C>G	XP_011530991.1:n.-80-25774C>G
XM_011532690.1:c.-80-25774C>G	XP_011530992.1:n.-80-25774C>G
XM_017003566.1:c.1858C>G	XP_016859055.1:p.Leu620Val
XM_024452745.1:c.1858C>G	XP_024308513.1:p.Leu620Val
XM_024452746.1:c.1858C>G	XP_024308514.1:p.Leu620Val
XM_024452747.1:c.-80-25774C>G	XP_024308515.1:n.-80-25774C>G