Canonical Allele Identifier: CA1433470610

Gene: TACC3

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1732438A= , CM000666.2:g.1732438A=	GRCh38
NC_000004.11:g.1734165A= , CM000666.1:g.1734165A=	GRCh37
NC_000004.10:g.1703963A=	NCBI36
NG_064424.1:g.15949A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000313288.9:c.1591+1137A= MANE Select	ENSP00000326550.4:n.1591+1137A=
ENST00000470136.2:c.520+1207A=
ENST00000612220.5:c.511+1137A=	ENSP00000478580.2:n.511+1137A=
ENST00000650779.1:n.1389+1137A=
ENST00000651251.1:n.1705+1137A=
ENST00000651472.1:c.1591+1137A=	ENSP00000498361.1:n.1591+1137A=
ENST00000651817.1:c.581+1137A=
ENST00000652770.1:c.1591+1137A=	ENSP00000498219.1:n.1591+1137A=
ENST00000313288.8:c.1591+1137A=	ENSP00000326550.4:n.1591+1137A=
ENST00000466077.1:n.290+1137A=
ENST00000470136.1:c.520+1207A=
ENST00000484651.5:n.1717+1137A=
ENST00000485989.6:c.511+1137A=	ENSP00000419210.2:n.511+1137A=
ENST00000612220.4:c.*74+1137A=	ENSP00000478580.1:n.*74+1137A=
ENST00000617535.4:c.*74+1137A=	ENSP00000483196.1:n.*74+1137A=
NM_006342.2:c.1591+1137A=	NP_006333.1:n.1591+1137A=
XM_005247929.1:c.1591+1137A=	XP_005247986.1:n.1591+1137A=
XM_005247930.1:c.511+1137A=	XP_005247987.1:n.511+1137A=
XM_011513386.1:c.1591+1137A=	XP_011511688.1:n.1591+1137A=
XM_011513387.1:c.1591+1137A=	XP_011511689.1:n.1591+1137A=
XM_005247929.3:c.1591+1137A=	XP_005247986.1:n.1591+1137A=
XM_005247930.3:c.511+1137A=	XP_005247987.1:n.511+1137A=
XM_011513386.3:c.1591+1137A=	XP_011511688.1:n.1591+1137A=
XM_017007653.1:c.1591+1137A=	XP_016863142.1:n.1591+1137A=
NM_006342.3:c.1591+1137A= MANE Select	NP_006333.1:n.1591+1137A=