Canonical Allele Identifier: CA10645875
Gene: MAPT HGNC NCBI
MAPT-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.45894541G>T , CM000679.2:g.45894541G>T GRCh38
NC_000017.10:g.43971907G>T , CM000679.1:g.43971907G>T GRCh37
NC_000017.9:g.41327701G>T NCBI36
NG_007398.1:g.5078G>T
NG_007398.2:g.5079G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001123066.3:c.-163G>T (MAPT) NP_001116538.2:n.-163G>T
NM_001123067.3:c.-163G>T (MAPT) NP_001116539.1:n.-163G>T
NM_001203251.1:c.-163G>T (MAPT) NP_001190180.1:n.-163G>T
NM_001203252.1:c.-163G>T (MAPT) NP_001190181.1:n.-163G>T
NM_005910.5:c.-163G>T (MAPT) NP_005901.2:n.-163G>T
NM_016834.4:c.-163G>T (MAPT) NP_058518.1:n.-163G>T
NM_016835.4:c.-163G>T (MAPT) NP_058519.3:n.-163G>T
NM_016841.4:c.-163G>T (MAPT) NP_058525.1:n.-163G>T
NR_024559.1:n.34+939C>A (MAPT-AS1)
ENST00000262410.9:c.-163G>T (MAPT) ENSP00000262410.5:n.-163G>T
ENST00000340799.9:c.-163G>T (MAPT) ENSP00000340438.5:n.-163G>T
ENST00000344290.9:c.-163G>T (MAPT) ENSP00000340820.5:n.-163G>T
ENST00000351559.9:c.-163G>T (MAPT) ENSP00000303214.7:n.-163G>T
ENST00000535772.5:c.-163G>T (MAPT) ENSP00000443028.1:n.-163G>T
ENST00000680674.1:c.-163G>T (MAPT) ENSP00000505478.1:n.-163G>T
ENST00000703922.1:c.-163G>T (MAPT) ENSP00000515557.1:n.-163G>T
ENST00000703923.1:c.-163G>T (MAPT) ENSP00000515558.1:n.-163G>T
ENST00000703924.1:c.-163G>T (MAPT) ENSP00000515559.1:n.-163G>T
XM_005257370.4:c.-163G>T (MAPT) XP_005257427.1:n.-163G>T