Canonical Allele Identifier: CA2262102722
Gene: MAPT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.46014292G= , CM000679.2:g.46014292G= GRCh38
NC_000017.10:g.44091658G= , CM000679.1:g.44091658G= GRCh37
NC_000017.9:g.41447495G= NCBI36
NG_007398.1:g.124872G=
NG_007398.2:g.124830G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000420682.7:c.878G= ENSP00000413056.2:p.Cys293=
ENST00000703922.1:c.878G= ENSP00000515557.1:p.Cys293=
ENST00000703923.1:c.791G= ENSP00000515558.1:p.Cys264=
ENST00000703924.1:c.878G= ENSP00000515559.1:p.Cys293=
ENST00000703978.1:c.965G= ENSP00000515600.1:p.Cys322=
ENST00000703979.1:n.736G=
ENST00000703980.1:n.191G=
ENST00000703981.1:n.134G=
ENST00000262410.10:c.2141G= MANE Select ENSP00000262410.6:p.Cys714=
ENST00000344290.10:c.1850G= ENSP00000340820.6:p.Cys617=
ENST00000351559.10:c.965G= ENSP00000303214.7:p.Cys322=
ENST00000535772.6:c.785G= ENSP00000443028.2:p.Cys262=
ENST00000680542.1:c.878G= ENSP00000505258.1:p.Cys293=
ENST00000680674.1:c.791G= ENSP00000505478.1:p.Cys264=
ENST00000262410.9:c.1916G= ENSP00000262410.5:p.Cys639=
ENST00000334239.12:c.698G= ENSP00000334886.8:p.Cys233=
ENST00000340799.9:c.878G= ENSP00000340438.5:p.Cys293=
ENST00000344290.9:c.1970G= ENSP00000340820.5:p.Cys657=
ENST00000351559.9:c.965G= ENSP00000303214.7:p.Cys322=
ENST00000415613.6:c.1970G= ENSP00000410838.2:p.Cys657=
ENST00000420682.6:c.878G= ENSP00000413056.2:p.Cys293=
ENST00000431008.7:c.872G= ENSP00000389250.3:p.Cys291=
ENST00000446361.7:c.791G= ENSP00000408975.3:p.Cys264=
ENST00000535772.5:c.872G= ENSP00000443028.1:p.Cys291=
ENST00000570299.5:n.777-4326G=
ENST00000571987.5:c.1916G= ENSP00000458742.1:p.Cys639=
ENST00000574436.5:c.965G= ENSP00000460965.1:p.Cys322=
ENST00000576518.1:n.6157G=
NM_001123066.3:c.1970G= NP_001116538.2:p.Cys657=
NM_001123067.3:c.878G= NP_001116539.1:p.Cys293=
NM_001203251.1:c.785G= NP_001190180.1:p.Cys262=
NM_001203252.1:c.872G= NP_001190181.1:p.Cys291=
NM_005910.5:c.965G= NP_005901.2:p.Cys322=
NM_016834.4:c.791G= NP_058518.1:p.Cys264=
NM_016835.4:c.1916G= NP_058519.3:p.Cys639=
NM_016841.4:c.698G= NP_058525.1:p.Cys233=
XM_005257362.3:c.2228G= XP_005257419.1:p.Cys743=
XM_005257364.3:c.2141G= XP_005257421.1:p.Cys714=
XM_005257365.3:c.2135G= XP_005257422.1:p.Cys712=
XM_005257366.2:c.2054G= XP_005257423.1:p.Cys685=
XM_005257367.3:c.2030G= XP_005257424.1:p.Cys677=
XM_005257368.3:c.1937G= XP_005257425.1:p.Cys646=
XM_005257369.3:c.1163G= XP_005257426.1:p.Cys388=
XM_005257370.3:c.1076G= XP_005257427.1:p.Cys359=
XM_005257371.3:c.989G= XP_005257428.1:p.Cys330=
XM_005257362.4:c.2228G= XP_005257419.1:p.Cys743=
XM_005257364.4:c.2141G= XP_005257421.1:p.Cys714=
XM_005257365.4:c.2135G= XP_005257422.1:p.Cys712=
XM_005257366.3:c.2054G= XP_005257423.1:p.Cys685=
XM_005257367.4:c.2030G= XP_005257424.1:p.Cys677=
XM_005257368.4:c.1937G= XP_005257425.1:p.Cys646=
XM_005257369.4:c.1163G= XP_005257426.1:p.Cys388=
XM_005257370.4:c.1076G= XP_005257427.1:p.Cys359=
XM_005257371.4:c.989G= XP_005257428.1:p.Cys330=
NM_001203251.2:c.785G= NP_001190180.1:p.Cys262=
NM_001377265.1:c.2141G= MANE Select NP_001364194.1:p.Cys714=
NM_001377266.1:c.1850G= NP_001364195.1:p.Cys617=
NM_001377267.1:c.771+14G= NP_001364196.1:n.771+14G=
NM_001377268.1:c.698G= NP_001364197.1:p.Cys233=
NM_016834.5:c.791G= NP_058518.1:p.Cys264=
NM_016841.5:c.698G= NP_058525.1:p.Cys233=
NR_165166.1:n.796G=
NM_001123066.4:c.1970G= NP_001116538.2:p.Cys657=
NM_001123067.4:c.878G= NP_001116539.1:p.Cys293=
NM_001203252.2:c.872G= NP_001190181.1:p.Cys291=
NM_005910.6:c.965G= NP_005901.2:p.Cys322=
NM_016835.5:c.1916G= NP_058519.3:p.Cys639=