Canonical Allele Identifier: CA2638367472

Gene: MAPT

Linked Data

• gnomAD v4: 17-46014338-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46014338A>C , CM000679.2:g.46014338A>C	GRCh38
NC_000017.10:g.44091704A>C , CM000679.1:g.44091704A>C	GRCh37
NC_000017.9:g.41447541A>C	NCBI36
NG_007398.1:g.124918A>C
NG_007398.2:g.124876A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.910+14A>C	ENSP00000413056.2:n.910+14A>C
ENST00000703922.1:c.910+14A>C	ENSP00000515557.1:n.910+14A>C
ENST00000703923.1:c.823+14A>C	ENSP00000515558.1:n.823+14A>C
ENST00000703924.1:c.910+14A>C	ENSP00000515559.1:n.910+14A>C
ENST00000703978.1:c.997+14A>C	ENSP00000515600.1:n.997+14A>C
ENST00000703979.1:n.768+14A>C
ENST00000703980.1:n.223+14A>C
ENST00000703981.1:n.180A>C
ENST00000262410.10:c.2173+14A>C MANE Select	ENSP00000262410.6:n.2173+14A>C
ENST00000344290.10:c.1882+14A>C	ENSP00000340820.6:n.1882+14A>C
ENST00000351559.10:c.997+14A>C	ENSP00000303214.7:n.997+14A>C
ENST00000535772.6:c.817+14A>C	ENSP00000443028.2:n.817+14A>C
ENST00000680542.1:c.910+14A>C	ENSP00000505258.1:n.910+14A>C
ENST00000680674.1:c.823+14A>C	ENSP00000505478.1:n.823+14A>C
ENST00000262410.9:c.1948+14A>C	ENSP00000262410.5:n.1948+14A>C
ENST00000334239.12:c.730+14A>C	ENSP00000334886.8:n.730+14A>C
ENST00000340799.9:c.910+14A>C	ENSP00000340438.5:n.910+14A>C
ENST00000344290.9:c.2002+14A>C	ENSP00000340820.5:n.2002+14A>C
ENST00000351559.9:c.997+14A>C	ENSP00000303214.7:n.997+14A>C
ENST00000415613.6:c.2002+14A>C	ENSP00000410838.2:n.2002+14A>C
ENST00000420682.6:c.910+14A>C	ENSP00000413056.2:n.910+14A>C
ENST00000431008.7:c.904+14A>C	ENSP00000389250.3:n.904+14A>C
ENST00000446361.7:c.823+14A>C	ENSP00000408975.3:n.823+14A>C
ENST00000535772.5:c.904+14A>C	ENSP00000443028.1:n.904+14A>C
ENST00000570299.5:n.777-4280A>C
ENST00000571987.5:c.1948+14A>C	ENSP00000458742.1:n.1948+14A>C
ENST00000574436.5:c.997+14A>C	ENSP00000460965.1:n.997+14A>C
ENST00000576518.1:n.6189+14A>C
NM_001123066.3:c.2002+14A>C	NP_001116538.2:n.2002+14A>C
NM_001123067.3:c.910+14A>C	NP_001116539.1:n.910+14A>C
NM_001203251.1:c.817+14A>C	NP_001190180.1:n.817+14A>C
NM_001203252.1:c.904+14A>C	NP_001190181.1:n.904+14A>C
NM_005910.5:c.997+14A>C	NP_005901.2:n.997+14A>C
NM_016834.4:c.823+14A>C	NP_058518.1:n.823+14A>C
NM_016835.4:c.1948+14A>C	NP_058519.3:n.1948+14A>C
NM_016841.4:c.730+14A>C	NP_058525.1:n.730+14A>C
XM_005257362.3:c.2260+14A>C	XP_005257419.1:n.2260+14A>C
XM_005257364.3:c.2173+14A>C	XP_005257421.1:n.2173+14A>C
XM_005257365.3:c.2167+14A>C	XP_005257422.1:n.2167+14A>C
XM_005257366.2:c.2086+14A>C	XP_005257423.1:n.2086+14A>C
XM_005257367.3:c.2062+14A>C	XP_005257424.1:n.2062+14A>C
XM_005257368.3:c.1969+14A>C	XP_005257425.1:n.1969+14A>C
XM_005257369.3:c.1195+14A>C	XP_005257426.1:n.1195+14A>C
XM_005257370.3:c.1108+14A>C	XP_005257427.1:n.1108+14A>C
XM_005257371.3:c.1021+14A>C	XP_005257428.1:n.1021+14A>C
XM_005257362.4:c.2260+14A>C	XP_005257419.1:n.2260+14A>C
XM_005257364.4:c.2173+14A>C	XP_005257421.1:n.2173+14A>C
XM_005257365.4:c.2167+14A>C	XP_005257422.1:n.2167+14A>C
XM_005257366.3:c.2086+14A>C	XP_005257423.1:n.2086+14A>C
XM_005257367.4:c.2062+14A>C	XP_005257424.1:n.2062+14A>C
XM_005257368.4:c.1969+14A>C	XP_005257425.1:n.1969+14A>C
XM_005257369.4:c.1195+14A>C	XP_005257426.1:n.1195+14A>C
XM_005257370.4:c.1108+14A>C	XP_005257427.1:n.1108+14A>C
XM_005257371.4:c.1021+14A>C	XP_005257428.1:n.1021+14A>C
NM_001203251.2:c.817+14A>C	NP_001190180.1:n.817+14A>C
NM_001377265.1:c.2173+14A>C MANE Select	NP_001364194.1:n.2173+14A>C
NM_001377266.1:c.1882+14A>C	NP_001364195.1:n.1882+14A>C
NM_001377267.1:c.771+60A>C	NP_001364196.1:n.771+60A>C
NM_001377268.1:c.730+14A>C	NP_001364197.1:n.730+14A>C
NM_016834.5:c.823+14A>C	NP_058518.1:n.823+14A>C
NM_016841.5:c.730+14A>C	NP_058525.1:n.730+14A>C
NR_165166.1:n.828+14A>C
NM_001123066.4:c.2002+14A>C	NP_001116538.2:n.2002+14A>C
NM_001123067.4:c.910+14A>C	NP_001116539.1:n.910+14A>C
NM_001203252.2:c.904+14A>C	NP_001190181.1:n.904+14A>C
NM_005910.6:c.997+14A>C	NP_005901.2:n.997+14A>C
NM_016835.5:c.1948+14A>C	NP_058519.3:n.1948+14A>C