Canonical Allele Identifier: CA410683129

Gene: TBX1

Linked Data

• MyVariant Identifiers: chr22:g.19751820A>T (hg19) ; chr22:g.19764297A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19764297A>T , CM000684.2:g.19764297A>T	GRCh38
NC_000022.10:g.19751820A>T , CM000684.1:g.19751820A>T	GRCh37
NC_000022.9:g.18131820A>T	NCBI36
NG_009229.1:g.12595A>T , LRG_226:g.12595A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700274.1:c.208A>T	ENSP00000514909.1:p.Thr70Ser
ENST00000649276.2:c.682A>T MANE Select	ENSP00000497003.1:p.Thr228Ser
ENST00000680333.1:c.655A>T	ENSP00000505472.1:p.Thr219Ser
ENST00000329705.11:c.655A>T	ENSP00000331176.7:p.Thr219Ser
ENST00000332710.8:c.655A>T	ENSP00000331791.4:p.Thr219Ser
ENST00000359500.7:c.655A>T	ENSP00000352483.3:p.Thr219Ser
ENST00000621939.1:c.655A>T	ENSP00000477982.1:p.Thr219Ser
NM_005992.1:c.655A>T	NP_005983.1:p.Thr219Ser
NM_080646.1:c.655A>T	NP_542377.1:p.Thr219Ser
NM_080647.1:c.655A>T , LRG_226t1:c.655A>T	NP_542378.1:p.Thr219Ser
XM_006724312.1:c.655A>T	XP_006724375.1:p.Thr219Ser
XM_011530351.1:c.682A>T	XP_011528653.1:p.Thr228Ser
XM_006724312.2:c.655A>T	XP_006724375.1:p.Thr219Ser
XM_017028925.1:c.805A>T	XP_016884414.1:p.Thr269Ser
XM_017028926.1:c.655A>T	XP_016884415.1:p.Thr219Ser
XM_017028928.1:c.805A>T	XP_016884417.1:p.Thr269Ser
NM_001379200.1:c.682A>T MANE Select	NP_001366129.1:p.Thr228Ser
NM_080646.2:c.655A>T	NP_542377.1:p.Thr219Ser