Canonical Allele Identifier: CA2269031003

Gene: TBX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61455988C= , CM000679.2:g.61455988C=	GRCh38
NC_000017.10:g.59533349C= , CM000679.1:g.59533349C=	GRCh37
NC_000017.9:g.56888131C=	NCBI36
NG_008080.1:g.4543C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644296.1:c.-3-500C= MANE Select	ENSP00000495986.1:n.-3-500C=
ENST00000393853.8:c.-3-500C=	ENSP00000377435.3:n.-3-500C=
ENST00000589003.5:c.-125-636C=	ENSP00000467588.1:n.-125-636C=
XM_005257835.3:c.-3-500C=	XP_005257892.2:n.-3-500C=
XM_005257837.2:c.-3-500C=	XP_005257894.1:n.-3-500C=
XM_011525490.1:c.187-500C=	XP_011523792.1:n.187-500C=
XM_011525491.1:c.187-500C=	XP_011523793.1:n.187-500C=
XM_011525492.1:c.-3-500C=	XP_011523794.1:n.-3-500C=
XM_011525493.1:c.-3-500C=	XP_011523795.1:n.-3-500C=
XM_011525494.1:c.-4+253C=	XP_011523796.1:n.-4+253C=
XM_011525495.1:c.187-500C=	XP_011523797.1:n.187-500C=
NM_001321120.2:c.-3-500C= MANE Select	NP_001308049.1:n.-3-500C=
XM_011525490.2:c.187-500C=	XP_011523792.1:n.187-500C=
XM_011525491.2:c.187-500C=	XP_011523793.1:n.187-500C=
XM_011525495.2:c.187-500C=	XP_011523797.1:n.187-500C=