Canonical Allele Identifier: CA399983460

Gene: MAPT

Linked Data

• MyVariant Identifiers: chr17:g.44091627C>T (hg19) ; chr17:g.46014261C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.46014261C>T , CM000679.2:g.46014261C>T	GRCh38
NC_000017.10:g.44091627C>T , CM000679.1:g.44091627C>T	GRCh37
NC_000017.9:g.41447464C>T	NCBI36
NG_007398.1:g.124841C>T
NG_007398.2:g.124799C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000420682.7:c.847C>T	ENSP00000413056.2:p.Pro283Ser
ENST00000703922.1:c.847C>T	ENSP00000515557.1:p.Pro283Ser
ENST00000703923.1:c.760C>T	ENSP00000515558.1:p.Pro254Ser
ENST00000703924.1:c.847C>T	ENSP00000515559.1:p.Pro283Ser
ENST00000703978.1:c.934C>T	ENSP00000515600.1:p.Pro312Ser
ENST00000703979.1:n.705C>T
ENST00000703980.1:n.160C>T
ENST00000703981.1:n.103C>T
ENST00000262410.10:c.2110C>T MANE Select	ENSP00000262410.6:p.Pro704Ser
ENST00000344290.10:c.1819C>T	ENSP00000340820.6:p.Pro607Ser
ENST00000351559.10:c.934C>T	ENSP00000303214.7:p.Pro312Ser
ENST00000535772.6:c.754C>T	ENSP00000443028.2:p.Pro252Ser
ENST00000680542.1:c.847C>T	ENSP00000505258.1:p.Pro283Ser
ENST00000680674.1:c.760C>T	ENSP00000505478.1:p.Pro254Ser
ENST00000262410.9:c.1885C>T	ENSP00000262410.5:p.Pro629Ser
ENST00000334239.12:c.667C>T	ENSP00000334886.8:p.Pro223Ser
ENST00000340799.9:c.847C>T	ENSP00000340438.5:p.Pro283Ser
ENST00000344290.9:c.1939C>T	ENSP00000340820.5:p.Pro647Ser
ENST00000351559.9:c.934C>T	ENSP00000303214.7:p.Pro312Ser
ENST00000415613.6:c.1939C>T	ENSP00000410838.2:p.Pro647Ser
ENST00000420682.6:c.847C>T	ENSP00000413056.2:p.Pro283Ser
ENST00000431008.7:c.841C>T	ENSP00000389250.3:p.Pro281Ser
ENST00000446361.7:c.760C>T	ENSP00000408975.3:p.Pro254Ser
ENST00000535772.5:c.841C>T	ENSP00000443028.1:p.Pro281Ser
ENST00000570299.5:n.777-4357C>T
ENST00000571987.5:c.1885C>T	ENSP00000458742.1:p.Pro629Ser
ENST00000574436.5:c.934C>T	ENSP00000460965.1:p.Pro312Ser
ENST00000576518.1:n.6126C>T
NM_001123066.3:c.1939C>T	NP_001116538.2:p.Pro647Ser
NM_001123067.3:c.847C>T	NP_001116539.1:p.Pro283Ser
NM_001203251.1:c.754C>T	NP_001190180.1:p.Pro252Ser
NM_001203252.1:c.841C>T	NP_001190181.1:p.Pro281Ser
NM_005910.5:c.934C>T	NP_005901.2:p.Pro312Ser
NM_016834.4:c.760C>T	NP_058518.1:p.Pro254Ser
NM_016835.4:c.1885C>T	NP_058519.3:p.Pro629Ser
NM_016841.4:c.667C>T	NP_058525.1:p.Pro223Ser
XM_005257362.3:c.2197C>T	XP_005257419.1:p.Pro733Ser
XM_005257364.3:c.2110C>T	XP_005257421.1:p.Pro704Ser
XM_005257365.3:c.2104C>T	XP_005257422.1:p.Pro702Ser
XM_005257366.2:c.2023C>T	XP_005257423.1:p.Pro675Ser
XM_005257367.3:c.1999C>T	XP_005257424.1:p.Pro667Ser
XM_005257368.3:c.1906C>T	XP_005257425.1:p.Pro636Ser
XM_005257369.3:c.1132C>T	XP_005257426.1:p.Pro378Ser
XM_005257370.3:c.1045C>T	XP_005257427.1:p.Pro349Ser
XM_005257371.3:c.958C>T	XP_005257428.1:p.Pro320Ser
XM_005257362.4:c.2197C>T	XP_005257419.1:p.Pro733Ser
XM_005257364.4:c.2110C>T	XP_005257421.1:p.Pro704Ser
XM_005257365.4:c.2104C>T	XP_005257422.1:p.Pro702Ser
XM_005257366.3:c.2023C>T	XP_005257423.1:p.Pro675Ser
XM_005257367.4:c.1999C>T	XP_005257424.1:p.Pro667Ser
XM_005257368.4:c.1906C>T	XP_005257425.1:p.Pro636Ser
XM_005257369.4:c.1132C>T	XP_005257426.1:p.Pro378Ser
XM_005257370.4:c.1045C>T	XP_005257427.1:p.Pro349Ser
XM_005257371.4:c.958C>T	XP_005257428.1:p.Pro320Ser
NM_001203251.2:c.754C>T	NP_001190180.1:p.Pro252Ser
NM_001377265.1:c.2110C>T MANE Select	NP_001364194.1:p.Pro704Ser
NM_001377266.1:c.1819C>T	NP_001364195.1:p.Pro607Ser
NM_001377267.1:c.754C>T	NP_001364196.1:p.Pro252Ser
NM_001377268.1:c.667C>T	NP_001364197.1:p.Pro223Ser
NM_016834.5:c.760C>T	NP_058518.1:p.Pro254Ser
NM_016841.5:c.667C>T	NP_058525.1:p.Pro223Ser
NR_165166.1:n.765C>T
NM_001123066.4:c.1939C>T	NP_001116538.2:p.Pro647Ser
NM_001123067.4:c.847C>T	NP_001116539.1:p.Pro283Ser
NM_001203252.2:c.841C>T	NP_001190181.1:p.Pro281Ser
NM_005910.6:c.934C>T	NP_005901.2:p.Pro312Ser
NM_016835.5:c.1885C>T	NP_058519.3:p.Pro629Ser