Canonical Allele Identifier: CA501138910

Gene: TBX4

Linked Data

• gnomAD v4: 17-61456667-C-A
• MyVariant Identifiers: chr17:g.59534028C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61456667C>A , CM000679.2:g.61456667C>A	GRCh38
NC_000017.10:g.59534028C>A , CM000679.1:g.59534028C>A	GRCh37
NC_000017.9:g.56888810C>A	NCBI36
NG_008080.1:g.5222C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642491.1:c.177C>A	ENSP00000495714.1:p.Ala59=
ENST00000644296.1:c.177C>A MANE Select	ENSP00000495986.1:p.Ala59=
ENST00000240335.1:c.177C>A	ENSP00000240335.1:p.Ala59=
ENST00000393853.8:c.177C>A	ENSP00000377435.3:p.Ala59=
ENST00000589003.5:c.-82C>A	ENSP00000467588.1:n.-82C>A
NM_018488.2:c.177C>A	NP_060958.2:p.Ala59=
XM_005257835.3:c.177C>A	XP_005257892.2:p.Ala59=
XM_005257837.2:c.177C>A	XP_005257894.1:p.Ala59=
XM_011525490.1:c.366C>A	XP_011523792.1:p.Ala122=
XM_011525491.1:c.366C>A	XP_011523793.1:p.Ala122=
XM_011525492.1:c.177C>A	XP_011523794.1:p.Ala59=
XM_011525493.1:c.177C>A	XP_011523795.1:p.Ala59=
XM_011525494.1:c.177C>A	XP_011523796.1:p.Ala59=
XM_011525495.1:c.366C>A	XP_011523797.1:p.Ala122=
NM_001321120.2:c.177C>A MANE Select	NP_001308049.1:p.Ala59=
NM_018488.3:c.177C>A	NP_060958.2:p.Ala59=
XM_011525490.2:c.366C>A	XP_011523792.1:p.Ala122=
XM_011525491.2:c.366C>A	XP_011523793.1:p.Ala122=
XM_011525495.2:c.366C>A	XP_011523797.1:p.Ala122=