Canonical Allele Identifier: CA2262108485

Gene: MAPT

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46027266_46027270delinsAGCCT , CM000679.2:g.46027266_46027270delinsAGCCT	GRCh38
NC_000017.10:g.44104632_44104636delinsAGCCT , CM000679.1:g.44104632_44104636delinsAGCCT	GRCh37
NC_000017.9:g.41460479_41460483delinsAGCCT	NCBI36
NG_007398.1:g.137856_137860delinsAGCCT
NG_007398.2:g.137804_137808delinsAGCCT

Transcript Alleles

HGVS	Amino-acid change
ENST00000262410.10:c.*3095_*3099delinsAGCCT MANE Select	ENSP00000262410.6:n.*3095_*3099delinsAGCC...
ENST00000351559.10:c.*3095_*3099delinsAGCCT	ENSP00000303214.7:n.*3095_*3099delinsAGCC...
ENST00000262410.9:c.*3095_*3099delinsAGCCT	ENSP00000262410.5:n.*3095_*3099delinsAGCC...
ENST00000340799.9:c.*3095_*3099delinsAGCCT	ENSP00000340438.5:n.*3095_*3099delinsAGCC...
ENST00000344290.9:c.*3095_*3099delinsAGCCT	ENSP00000340820.5:n.*3095_*3099delinsAGCC...
ENST00000351559.9:c.*3095_*3099delinsAGCCT	ENSP00000303214.7:n.*3095_*3099delinsAGCC...
ENST00000446361.7:c.*3095_*3099delinsAGCCT	ENSP00000408975.3:n.*3095_*3099delinsAGCC...
ENST00000535772.5:c.*3095_*3099delinsAGCCT	ENSP00000443028.1:n.*3095_*3099delinsAGCC...
NM_001123066.3:c.*3095_*3099delinsAGCCT	NP_001116538.2:n.*3095_*3099delinsAGCCT
NM_001123067.3:c.*3095_*3099delinsAGCCT	NP_001116539.1:n.*3095_*3099delinsAGCCT
NM_001203251.1:c.*3095_*3099delinsAGCCT	NP_001190180.1:n.*3095_*3099delinsAGCCT
NM_001203252.1:c.*3095_*3099delinsAGCCT	NP_001190181.1:n.*3095_*3099delinsAGCCT
NM_005910.5:c.*3095_*3099delinsAGCCT	NP_005901.2:n.*3095_*3099delinsAGCCT
NM_016834.4:c.*3095_*3099delinsAGCCT	NP_058518.1:n.*3095_*3099delinsAGCCT
NM_016835.4:c.*3095_*3099delinsAGCCT	NP_058519.3:n.*3095_*3099delinsAGCCT
NM_016841.4:c.*3095_*3099delinsAGCCT	NP_058525.1:n.*3095_*3099delinsAGCCT
XM_005257362.4:c.*3095_*3099delinsAGCCT	XP_005257419.1:n.*3095_*3099delinsAGCCT
XM_005257364.4:c.*3095_*3099delinsAGCCT	XP_005257421.1:n.*3095_*3099delinsAGCCT
XM_005257365.4:c.*3095_*3099delinsAGCCT	XP_005257422.1:n.*3095_*3099delinsAGCCT
XM_005257366.3:c.*3095_*3099delinsAGCCT	XP_005257423.1:n.*3095_*3099delinsAGCCT
XM_005257367.4:c.*3095_*3099delinsAGCCT	XP_005257424.1:n.*3095_*3099delinsAGCCT
XM_005257368.4:c.*3095_*3099delinsAGCCT	XP_005257425.1:n.*3095_*3099delinsAGCCT
XM_005257369.4:c.*3095_*3099delinsAGCCT	XP_005257426.1:n.*3095_*3099delinsAGCCT
XM_005257370.4:c.*3095_*3099delinsAGCCT	XP_005257427.1:n.*3095_*3099delinsAGCCT
XM_005257371.4:c.*3095_*3099delinsAGCCT	XP_005257428.1:n.*3095_*3099delinsAGCCT
NM_001203251.2:c.*3095_*3099delinsAGCCT	NP_001190180.1:n.*3095_*3099delinsAGCCT
NM_001377265.1:c.*3095_*3099delinsAGCCT MANE Select	NP_001364194.1:n.*3095_*3099delinsAGCCT
NM_001377266.1:c.*3095_*3099delinsAGCCT	NP_001364195.1:n.*3095_*3099delinsAGCCT
NM_001377267.1:c.*2078_*2082delinsAGCCT	NP_001364196.1:n.*2078_*2082delinsAGCCT
NM_001377268.1:c.*3095_*3099delinsAGCCT	NP_001364197.1:n.*3095_*3099delinsAGCCT
NM_016834.5:c.*3095_*3099delinsAGCCT	NP_058518.1:n.*3095_*3099delinsAGCCT
NM_016841.5:c.*3095_*3099delinsAGCCT	NP_058525.1:n.*3095_*3099delinsAGCCT
NR_165166.1:n.4252_4256delinsAGCCT
NM_001123066.4:c.*3095_*3099delinsAGCCT	NP_001116538.2:n.*3095_*3099delinsAGCCT
NM_001123067.4:c.*3095_*3099delinsAGCCT	NP_001116539.1:n.*3095_*3099delinsAGCCT
NM_001203252.2:c.*3095_*3099delinsAGCCT	NP_001190181.1:n.*3095_*3099delinsAGCCT
NM_005910.6:c.*3095_*3099delinsAGCCT	NP_005901.2:n.*3095_*3099delinsAGCCT
NM_016835.5:c.*3095_*3099delinsAGCCT	NP_058519.3:n.*3095_*3099delinsAGCCT