Canonical Allele Identifier: CA400469180

Gene: TBX4

Linked Data

• gnomAD v4: 17-61456663-C-T
• MyVariant Identifiers: chr17:g.59534024C>T (hg19) ; chr17:g.61456663C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.61456663C>T , CM000679.2:g.61456663C>T	GRCh38
NC_000017.10:g.59534024C>T , CM000679.1:g.59534024C>T	GRCh37
NC_000017.9:g.56888806C>T	NCBI36
NG_008080.1:g.5218C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642491.1:c.173C>T	ENSP00000495714.1:p.Ala58Val
ENST00000644296.1:c.173C>T MANE Select	ENSP00000495986.1:p.Ala58Val
ENST00000240335.1:c.173C>T	ENSP00000240335.1:p.Ala58Val
ENST00000393853.8:c.173C>T	ENSP00000377435.3:p.Ala58Val
ENST00000589003.5:c.-86C>T	ENSP00000467588.1:n.-86C>T
NM_018488.2:c.173C>T	NP_060958.2:p.Ala58Val
XM_005257835.3:c.173C>T	XP_005257892.2:p.Ala58Val
XM_005257837.2:c.173C>T	XP_005257894.1:p.Ala58Val
XM_011525490.1:c.362C>T	XP_011523792.1:p.Ala121Val
XM_011525491.1:c.362C>T	XP_011523793.1:p.Ala121Val
XM_011525492.1:c.173C>T	XP_011523794.1:p.Ala58Val
XM_011525493.1:c.173C>T	XP_011523795.1:p.Ala58Val
XM_011525494.1:c.173C>T	XP_011523796.1:p.Ala58Val
XM_011525495.1:c.362C>T	XP_011523797.1:p.Ala121Val
NM_001321120.2:c.173C>T MANE Select	NP_001308049.1:p.Ala58Val
NM_018488.3:c.173C>T	NP_060958.2:p.Ala58Val
XM_011525490.2:c.362C>T	XP_011523792.1:p.Ala121Val
XM_011525491.2:c.362C>T	XP_011523793.1:p.Ala121Val
XM_011525495.2:c.362C>T	XP_011523797.1:p.Ala121Val