Canonical Allele Identifier: CA549173614

Gene: TACC3

Linked Data

• gnomAD v2: 4-1733987-GGTTTGTCCGTAAGATTGGAGGCTGCAGTTAAATAAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTGAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTGAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTAAATAAATACA-G
• gnomAD v3: 4-1732260-GGTTTGTCCGTAAGATTGGAGGCTGCAGTTAAATAAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTGAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTGAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTAAATAAATACA-G
• gnomAD v4: 4-1732260-GGTTTGTCCGTAAGATTGGAGGCTGCAGTTAAATAAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTGAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTGAATACGGTTTGTCCGTAAGATTGGAGGCTGCAGTTAAATAAATACA-G
• MyVariant Identifiers: chr4:g.1733988_1734139del (hg19) ; chr4:g.1732261_1732412del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1732320_1732471del , CM000666.2:g.1732320_1732471del	GRCh38
NC_000004.11:g.1734047_1734198del , CM000666.1:g.1734047_1734198del	GRCh37
NC_000004.10:g.1703845_1703996del	NCBI36
NG_064424.1:g.15831_15982del

Transcript Alleles

HGVS	Amino-acid change
ENST00000313288.9:c.1591+1019_1591+1170del MANE Select	ENSP00000326550.4:n.1591+1019_1591+1170del
ENST00000470136.2:c.520+1089_520+1240del
ENST00000612220.5:c.511+1019_511+1170del	ENSP00000478580.2:n.511+1019_511+1170del
ENST00000650779.1:n.1389+1019_1389+1170del
ENST00000651251.1:n.1705+1019_1705+1170del
ENST00000651472.1:c.1591+1019_1591+1170del	ENSP00000498361.1:n.1591+1019_1591+1170del
ENST00000651817.1:c.581+1019_581+1170del
ENST00000652770.1:c.1591+1019_1591+1170del	ENSP00000498219.1:n.1591+1019_1591+1170del
ENST00000313288.8:c.1591+1019_1591+1170del	ENSP00000326550.4:n.1591+1019_1591+1170del
ENST00000466077.1:n.290+1019_290+1170del
ENST00000470136.1:c.520+1089_520+1240del
ENST00000484651.5:n.1717+1019_1717+1170del
ENST00000485989.6:c.511+1019_511+1170del	ENSP00000419210.2:n.511+1019_511+1170del
ENST00000612220.4:c.*74+1019_*74+1170del	ENSP00000478580.1:n.*74+1019_*74+1170del
ENST00000617535.4:c.*74+1019_*74+1170del	ENSP00000483196.1:n.*74+1019_*74+1170del
NM_006342.2:c.1591+1019_1591+1170del	NP_006333.1:n.1591+1019_1591+1170del
XM_005247929.1:c.1591+1019_1591+1170del	XP_005247986.1:n.1591+1019_1591+1170del
XM_005247930.1:c.511+1019_511+1170del	XP_005247987.1:n.511+1019_511+1170del
XM_011513386.1:c.1591+1019_1591+1170del	XP_011511688.1:n.1591+1019_1591+1170del
XM_011513387.1:c.1591+1019_1591+1170del	XP_011511689.1:n.1591+1019_1591+1170del
XM_005247929.3:c.1591+1019_1591+1170del	XP_005247986.1:n.1591+1019_1591+1170del
XM_005247930.3:c.511+1019_511+1170del	XP_005247987.1:n.511+1019_511+1170del
XM_011513386.3:c.1591+1019_1591+1170del	XP_011511688.1:n.1591+1019_1591+1170del
XM_017007653.1:c.1591+1019_1591+1170del	XP_016863142.1:n.1591+1019_1591+1170del
NM_006342.3:c.1591+1019_1591+1170del MANE Select	NP_006333.1:n.1591+1019_1591+1170del