Canonical Allele Identifier: CA2269031004

Gene: TBX4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61455992C= , CM000679.2:g.61455992C=	GRCh38
NC_000017.10:g.59533353C= , CM000679.1:g.59533353C=	GRCh37
NC_000017.9:g.56888135C=	NCBI36
NG_008080.1:g.4547C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644296.1:c.-3-496C= MANE Select	ENSP00000495986.1:n.-3-496C=
ENST00000393853.8:c.-3-496C=	ENSP00000377435.3:n.-3-496C=
ENST00000589003.5:c.-125-632C=	ENSP00000467588.1:n.-125-632C=
XM_005257835.3:c.-3-496C=	XP_005257892.2:n.-3-496C=
XM_005257837.2:c.-3-496C=	XP_005257894.1:n.-3-496C=
XM_011525490.1:c.187-496C=	XP_011523792.1:n.187-496C=
XM_011525491.1:c.187-496C=	XP_011523793.1:n.187-496C=
XM_011525492.1:c.-3-496C=	XP_011523794.1:n.-3-496C=
XM_011525493.1:c.-3-496C=	XP_011523795.1:n.-3-496C=
XM_011525494.1:c.-4+257C=	XP_011523796.1:n.-4+257C=
XM_011525495.1:c.187-496C=	XP_011523797.1:n.187-496C=
NM_001321120.2:c.-3-496C= MANE Select	NP_001308049.1:n.-3-496C=
XM_011525490.2:c.187-496C=	XP_011523792.1:n.187-496C=
XM_011525491.2:c.187-496C=	XP_011523793.1:n.187-496C=
XM_011525495.2:c.187-496C=	XP_011523797.1:n.187-496C=