Canonical Allele Identifier: CA399983434

Gene: MAPT

Linked Data

• dbSNP Id: rs766611003
• MyVariant Identifiers: chr17:g.44091616T>C (hg19) ; chr17:g.46014250T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46014250T>C , CM000679.2:g.46014250T>C	GRCh38
NC_000017.10:g.44091616T>C , CM000679.1:g.44091616T>C	GRCh37
NC_000017.9:g.41447453T>C	NCBI36
NG_007398.1:g.124830T>C
NG_007398.2:g.124788T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.836T>C	ENSP00000413056.2:p.Ile279Thr
ENST00000703922.1:c.836T>C	ENSP00000515557.1:p.Ile279Thr
ENST00000703923.1:c.749T>C	ENSP00000515558.1:p.Ile250Thr
ENST00000703924.1:c.836T>C	ENSP00000515559.1:p.Ile279Thr
ENST00000703978.1:c.923T>C	ENSP00000515600.1:p.Ile308Thr
ENST00000703979.1:n.694T>C
ENST00000703980.1:n.149T>C
ENST00000703981.1:n.92T>C
ENST00000262410.10:c.2099T>C MANE Select	ENSP00000262410.6:p.Ile700Thr
ENST00000344290.10:c.1808T>C	ENSP00000340820.6:p.Ile603Thr
ENST00000351559.10:c.923T>C	ENSP00000303214.7:p.Ile308Thr
ENST00000535772.6:c.743T>C	ENSP00000443028.2:p.Ile248Thr
ENST00000680542.1:c.836T>C	ENSP00000505258.1:p.Ile279Thr
ENST00000680674.1:c.749T>C	ENSP00000505478.1:p.Ile250Thr
ENST00000262410.9:c.1874T>C	ENSP00000262410.5:p.Ile625Thr
ENST00000334239.12:c.656T>C	ENSP00000334886.8:p.Ile219Thr
ENST00000340799.9:c.836T>C	ENSP00000340438.5:p.Ile279Thr
ENST00000344290.9:c.1928T>C	ENSP00000340820.5:p.Ile643Thr
ENST00000351559.9:c.923T>C	ENSP00000303214.7:p.Ile308Thr
ENST00000415613.6:c.1928T>C	ENSP00000410838.2:p.Ile643Thr
ENST00000420682.6:c.836T>C	ENSP00000413056.2:p.Ile279Thr
ENST00000431008.7:c.830T>C	ENSP00000389250.3:p.Ile277Thr
ENST00000446361.7:c.749T>C	ENSP00000408975.3:p.Ile250Thr
ENST00000535772.5:c.830T>C	ENSP00000443028.1:p.Ile277Thr
ENST00000570299.5:n.777-4368T>C
ENST00000571987.5:c.1874T>C	ENSP00000458742.1:p.Ile625Thr
ENST00000574436.5:c.923T>C	ENSP00000460965.1:p.Ile308Thr
ENST00000576518.1:n.6115T>C
NM_001123066.3:c.1928T>C	NP_001116538.2:p.Ile643Thr
NM_001123067.3:c.836T>C	NP_001116539.1:p.Ile279Thr
NM_001203251.1:c.743T>C	NP_001190180.1:p.Ile248Thr
NM_001203252.1:c.830T>C	NP_001190181.1:p.Ile277Thr
NM_005910.5:c.923T>C	NP_005901.2:p.Ile308Thr
NM_016834.4:c.749T>C	NP_058518.1:p.Ile250Thr
NM_016835.4:c.1874T>C	NP_058519.3:p.Ile625Thr
NM_016841.4:c.656T>C	NP_058525.1:p.Ile219Thr
XM_005257362.3:c.2186T>C	XP_005257419.1:p.Ile729Thr
XM_005257364.3:c.2099T>C	XP_005257421.1:p.Ile700Thr
XM_005257365.3:c.2093T>C	XP_005257422.1:p.Ile698Thr
XM_005257366.2:c.2012T>C	XP_005257423.1:p.Ile671Thr
XM_005257367.3:c.1988T>C	XP_005257424.1:p.Ile663Thr
XM_005257368.3:c.1895T>C	XP_005257425.1:p.Ile632Thr
XM_005257369.3:c.1121T>C	XP_005257426.1:p.Ile374Thr
XM_005257370.3:c.1034T>C	XP_005257427.1:p.Ile345Thr
XM_005257371.3:c.947T>C	XP_005257428.1:p.Ile316Thr
XM_005257362.4:c.2186T>C	XP_005257419.1:p.Ile729Thr
XM_005257364.4:c.2099T>C	XP_005257421.1:p.Ile700Thr
XM_005257365.4:c.2093T>C	XP_005257422.1:p.Ile698Thr
XM_005257366.3:c.2012T>C	XP_005257423.1:p.Ile671Thr
XM_005257367.4:c.1988T>C	XP_005257424.1:p.Ile663Thr
XM_005257368.4:c.1895T>C	XP_005257425.1:p.Ile632Thr
XM_005257369.4:c.1121T>C	XP_005257426.1:p.Ile374Thr
XM_005257370.4:c.1034T>C	XP_005257427.1:p.Ile345Thr
XM_005257371.4:c.947T>C	XP_005257428.1:p.Ile316Thr
NM_001203251.2:c.743T>C	NP_001190180.1:p.Ile248Thr
NM_001377265.1:c.2099T>C MANE Select	NP_001364194.1:p.Ile700Thr
NM_001377266.1:c.1808T>C	NP_001364195.1:p.Ile603Thr
NM_001377267.1:c.743T>C	NP_001364196.1:p.Ile248Thr
NM_001377268.1:c.656T>C	NP_001364197.1:p.Ile219Thr
NM_016834.5:c.749T>C	NP_058518.1:p.Ile250Thr
NM_016841.5:c.656T>C	NP_058525.1:p.Ile219Thr
NR_165166.1:n.754T>C
NM_001123066.4:c.1928T>C	NP_001116538.2:p.Ile643Thr
NM_001123067.4:c.836T>C	NP_001116539.1:p.Ile279Thr
NM_001203252.2:c.830T>C	NP_001190181.1:p.Ile277Thr
NM_005910.6:c.923T>C	NP_005901.2:p.Ile308Thr
NM_016835.5:c.1874T>C	NP_058519.3:p.Ile625Thr