Canonical Allele Identifier: CA2262108892

Gene: MAPT KANSL1

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46028029A>T , CM000679.2:g.46028029A>T	GRCh38
NC_000017.10:g.44105395A>T , CM000679.1:g.44105395A>T	GRCh37
NG_032784.1:g.202346T>A
NG_007398.2:g.138567A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262410.10:c.*3858A>T (MAPT) MANE Select	ENSP00000262410.6:n.*3858A>T
ENST00000351559.10:c.*3858A>T (MAPT)	ENSP00000303214.7:n.*3858A>T
ENST00000262410.9:c.*3858A>T (MAPT)	ENSP00000262410.5:n.*3858A>T
ENST00000340799.9:c.*3858A>T (MAPT)	ENSP00000340438.5:n.*3858A>T
ENST00000344290.9:c.*3858A>T (MAPT)	ENSP00000340820.5:n.*3858A>T
ENST00000351559.9:c.*3858A>T (MAPT)	ENSP00000303214.7:n.*3858A>T
ENST00000446361.7:c.*3858A>T (MAPT)	ENSP00000408975.3:n.*3858A>T
ENST00000535772.5:c.*3858A>T (MAPT)	ENSP00000443028.1:n.*3858A>T
NM_001123066.3:c.*3858A>T (MAPT)	NP_001116538.2:n.*3858A>T
NM_001123067.3:c.*3858A>T (MAPT)	NP_001116539.1:n.*3858A>T
NM_001203251.1:c.*3858A>T (MAPT)	NP_001190180.1:n.*3858A>T
NM_001203252.1:c.*3858A>T (MAPT)	NP_001190181.1:n.*3858A>T
NM_005910.5:c.*3858A>T (MAPT)	NP_005901.2:n.*3858A>T
NM_016834.4:c.*3858A>T (MAPT)	NP_058518.1:n.*3858A>T
NM_016835.4:c.*3858A>T (MAPT)	NP_058519.3:n.*3858A>T
NM_016841.4:c.*3858A>T (MAPT)	NP_058525.1:n.*3858A>T
XM_005257362.4:c.*3858A>T (MAPT)	XP_005257419.1:n.*3858A>T
XM_005257364.4:c.*3858A>T (MAPT)	XP_005257421.1:n.*3858A>T
XM_005257365.4:c.*3858A>T (MAPT)	XP_005257422.1:n.*3858A>T
XM_005257366.3:c.*3858A>T (MAPT)	XP_005257423.1:n.*3858A>T
XM_005257367.4:c.*3858A>T (MAPT)	XP_005257424.1:n.*3858A>T
XM_005257368.4:c.*3858A>T (MAPT)	XP_005257425.1:n.*3858A>T
XM_005257369.4:c.*3858A>T (MAPT)	XP_005257426.1:n.*3858A>T
XM_005257370.4:c.*3858A>T (MAPT)	XP_005257427.1:n.*3858A>T
XM_005257371.4:c.*3858A>T (MAPT)	XP_005257428.1:n.*3858A>T
XM_006721824.4:c.*3447T>A (KANSL1)	XP_006721887.1:n.*3447T>A
XM_011524628.3:c.*3447T>A (KANSL1)	XP_011522930.1:n.*3447T>A
XM_011524630.3:c.*3447T>A (KANSL1)	XP_011522932.1:n.*3447T>A
XM_011524631.3:c.*3447T>A (KANSL1)	XP_011522933.1:n.*3447T>A
XM_017024488.2:c.*3447T>A (KANSL1)	XP_016879977.1:n.*3447T>A
NM_001203251.2:c.*3858A>T (MAPT)	NP_001190180.1:n.*3858A>T
NM_001377265.1:c.*3858A>T (MAPT) MANE Select	NP_001364194.1:n.*3858A>T
NM_001377266.1:c.*3858A>T (MAPT)	NP_001364195.1:n.*3858A>T
NM_001377267.1:c.*2841A>T (MAPT)	NP_001364196.1:n.*2841A>T
NM_001377268.1:c.*3858A>T (MAPT)	NP_001364197.1:n.*3858A>T
NM_016834.5:c.*3858A>T (MAPT)	NP_058518.1:n.*3858A>T
NM_016841.5:c.*3858A>T (MAPT)	NP_058525.1:n.*3858A>T
NR_165166.1:n.5015A>T (MAPT)
NM_001123066.4:c.*3858A>T (MAPT)	NP_001116538.2:n.*3858A>T
NM_001123067.4:c.*3858A>T (MAPT)	NP_001116539.1:n.*3858A>T
NM_001203252.2:c.*3858A>T (MAPT)	NP_001190181.1:n.*3858A>T
NM_005910.6:c.*3858A>T (MAPT)	NP_005901.2:n.*3858A>T
NM_016835.5:c.*3858A>T (MAPT)	NP_058519.3:n.*3858A>T