Canonical Allele Identifier: CA399984510

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44101440A>C (hg19) ; chr17:g.46024074A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46024074A>C , CM000679.2:g.46024074A>C	GRCh38
NC_000017.10:g.44101440A>C , CM000679.1:g.44101440A>C	GRCh37
NC_000017.9:g.41457285A>C	NCBI36
NG_007398.1:g.134662A>C
NG_007398.2:g.134612A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.1142A>C	ENSP00000413056.2:p.Asn381Thr
ENST00000703922.1:c.1142A>C	ENSP00000515557.1:p.Asn381Thr
ENST00000703923.1:c.1055A>C	ENSP00000515558.1:p.Asn352Thr
ENST00000703924.1:c.1142A>C	ENSP00000515559.1:p.Asn381Thr
ENST00000703978.1:c.1229A>C	ENSP00000515600.1:p.Asn410Thr
ENST00000703980.1:n.455A>C
ENST00000703981.1:n.413A>C
ENST00000703982.1:n.647A>C
ENST00000262410.10:c.2405A>C MANE Select	ENSP00000262410.6:p.Asn802Thr
ENST00000344290.10:c.2114A>C	ENSP00000340820.6:p.Asn705Thr
ENST00000351559.10:c.1229A>C	ENSP00000303214.7:p.Asn410Thr
ENST00000535772.6:c.1049A>C	ENSP00000443028.2:p.Asn350Thr
ENST00000680542.1:c.1142A>C	ENSP00000505258.1:p.Asn381Thr
ENST00000680674.1:c.1178A>C	ENSP00000505478.1:p.Asn393Thr
ENST00000262410.9:c.2180A>C	ENSP00000262410.5:p.Asn727Thr
ENST00000334239.12:c.962A>C	ENSP00000334886.8:p.Asn321Thr
ENST00000340799.9:c.1142A>C	ENSP00000340438.5:p.Asn381Thr
ENST00000344290.9:c.2234A>C	ENSP00000340820.5:p.Asn745Thr
ENST00000351559.9:c.1229A>C	ENSP00000303214.7:p.Asn410Thr
ENST00000415613.6:c.2234A>C	ENSP00000410838.2:p.Asn745Thr
ENST00000420682.6:c.1142A>C	ENSP00000413056.2:p.Asn381Thr
ENST00000431008.7:c.1136A>C	ENSP00000389250.3:p.Asn379Thr
ENST00000446361.7:c.1055A>C	ENSP00000408975.3:p.Asn352Thr
ENST00000535772.5:c.1136A>C	ENSP00000443028.1:p.Asn379Thr
ENST00000571987.5:c.2180A>C	ENSP00000458742.1:p.Asn727Thr
ENST00000574436.5:c.1229A>C	ENSP00000460965.1:p.Asn410Thr
ENST00000576518.1:n.6421A>C
NM_001123066.3:c.2234A>C	NP_001116538.2:p.Asn745Thr
NM_001123067.3:c.1142A>C	NP_001116539.1:p.Asn381Thr
NM_001203251.1:c.1049A>C	NP_001190180.1:p.Asn350Thr
NM_001203252.1:c.1136A>C	NP_001190181.1:p.Asn379Thr
NM_005910.5:c.1229A>C	NP_005901.2:p.Asn410Thr
NM_016834.4:c.1055A>C	NP_058518.1:p.Asn352Thr
NM_016835.4:c.2180A>C	NP_058519.3:p.Asn727Thr
NM_016841.4:c.962A>C	NP_058525.1:p.Asn321Thr
XM_005257362.3:c.2492A>C	XP_005257419.1:p.Asn831Thr
XM_005257364.3:c.2405A>C	XP_005257421.1:p.Asn802Thr
XM_005257365.3:c.2399A>C	XP_005257422.1:p.Asn800Thr
XM_005257366.2:c.2318A>C	XP_005257423.1:p.Asn773Thr
XM_005257367.3:c.2294A>C	XP_005257424.1:p.Asn765Thr
XM_005257368.3:c.2201A>C	XP_005257425.1:p.Asn734Thr
XM_005257369.3:c.1427A>C	XP_005257426.1:p.Asn476Thr
XM_005257370.3:c.1340A>C	XP_005257427.1:p.Asn447Thr
XM_005257371.3:c.1253A>C	XP_005257428.1:p.Asn418Thr
XM_005257362.4:c.2492A>C	XP_005257419.1:p.Asn831Thr
XM_005257364.4:c.2405A>C	XP_005257421.1:p.Asn802Thr
XM_005257365.4:c.2399A>C	XP_005257422.1:p.Asn800Thr
XM_005257366.3:c.2318A>C	XP_005257423.1:p.Asn773Thr
XM_005257367.4:c.2294A>C	XP_005257424.1:p.Asn765Thr
XM_005257368.4:c.2201A>C	XP_005257425.1:p.Asn734Thr
XM_005257369.4:c.1427A>C	XP_005257426.1:p.Asn476Thr
XM_005257370.4:c.1340A>C	XP_005257427.1:p.Asn447Thr
XM_005257371.4:c.1253A>C	XP_005257428.1:p.Asn418Thr
NM_001203251.2:c.1049A>C	NP_001190180.1:p.Asn350Thr
NM_001377265.1:c.2405A>C MANE Select	NP_001364194.1:p.Asn802Thr
NM_001377266.1:c.2114A>C	NP_001364195.1:p.Asn705Thr
NM_001377267.1:c.772-1043A>C	NP_001364196.1:n.772-1043A>C
NM_001377268.1:c.962A>C	NP_001364197.1:p.Asn321Thr
NM_016834.5:c.1055A>C	NP_058518.1:p.Asn352Thr
NM_016841.5:c.962A>C	NP_058525.1:p.Asn321Thr
NR_165166.1:n.1060A>C
NM_001123066.4:c.2234A>C	NP_001116538.2:p.Asn745Thr
NM_001123067.4:c.1142A>C	NP_001116539.1:p.Asn381Thr
NM_001203252.2:c.1136A>C	NP_001190181.1:p.Asn379Thr
NM_005910.6:c.1229A>C	NP_005901.2:p.Asn410Thr
NM_016835.5:c.2180A>C	NP_058519.3:p.Asn727Thr