Canonical Allele Identifier: CA1058513693

Gene: TACC3

Linked Data

• dbSNP Id: rs1718050187
• gnomAD v3: 4-1732440-TTAAA-T
• gnomAD v4: 4-1732440-TTAAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.1732447_1732450del , CM000666.2:g.1732447_1732450del	GRCh38
NC_000004.11:g.1734174_1734177del , CM000666.1:g.1734174_1734177del	GRCh37
NC_000004.10:g.1703972_1703975del	NCBI36
NG_064424.1:g.15958_15961del

Transcript Alleles

HGVS	Amino-acid change
ENST00000313288.9:c.1591+1146_1591+1149del MANE Select	ENSP00000326550.4:n.1591+1146_1591+1149de...
ENST00000470136.2:c.520+1216_520+1219del
ENST00000612220.5:c.511+1146_511+1149del	ENSP00000478580.2:n.511+1146_511+1149del
ENST00000650779.1:n.1389+1146_1389+1149del
ENST00000651251.1:n.1705+1146_1705+1149del
ENST00000651472.1:c.1591+1146_1591+1149del	ENSP00000498361.1:n.1591+1146_1591+1149de...
ENST00000651817.1:c.581+1146_581+1149del
ENST00000652770.1:c.1591+1146_1591+1149del	ENSP00000498219.1:n.1591+1146_1591+1149de...
ENST00000313288.8:c.1591+1146_1591+1149del	ENSP00000326550.4:n.1591+1146_1591+1149de...
ENST00000466077.1:n.290+1146_290+1149del
ENST00000470136.1:c.520+1216_520+1219del
ENST00000484651.5:n.1717+1146_1717+1149del
ENST00000485989.6:c.511+1146_511+1149del	ENSP00000419210.2:n.511+1146_511+1149del
ENST00000612220.4:c.*74+1146_*74+1149del	ENSP00000478580.1:n.*74+1146_*74+1149del
ENST00000617535.4:c.*74+1146_*74+1149del	ENSP00000483196.1:n.*74+1146_*74+1149del
NM_006342.2:c.1591+1146_1591+1149del	NP_006333.1:n.1591+1146_1591+1149del
XM_005247929.1:c.1591+1146_1591+1149del	XP_005247986.1:n.1591+1146_1591+1149del
XM_005247930.1:c.511+1146_511+1149del	XP_005247987.1:n.511+1146_511+1149del
XM_011513386.1:c.1591+1146_1591+1149del	XP_011511688.1:n.1591+1146_1591+1149del
XM_011513387.1:c.1591+1146_1591+1149del	XP_011511689.1:n.1591+1146_1591+1149del
XM_005247929.3:c.1591+1146_1591+1149del	XP_005247986.1:n.1591+1146_1591+1149del
XM_005247930.3:c.511+1146_511+1149del	XP_005247987.1:n.511+1146_511+1149del
XM_011513386.3:c.1591+1146_1591+1149del	XP_011511688.1:n.1591+1146_1591+1149del
XM_017007653.1:c.1591+1146_1591+1149del	XP_016863142.1:n.1591+1146_1591+1149del
NM_006342.3:c.1591+1146_1591+1149del MANE Select	NP_006333.1:n.1591+1146_1591+1149del