Canonical Allele Identifier: CA2396031425

Gene: TBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19764987G= , CM000684.2:g.19764987G=	GRCh38
NC_000022.10:g.19752510G= , CM000684.1:g.19752510G=	GRCh37
NC_000022.9:g.18132510G=	NCBI36
NG_009229.1:g.13285G= , LRG_226:g.13285G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700274.1:c.267G=	ENSP00000514909.1:p.Gln89=
ENST00000649276.2:c.741G= MANE Select	ENSP00000497003.1:p.Gln247=
ENST00000680333.1:c.714G=	ENSP00000505472.1:p.Gln238=
ENST00000329705.11:c.714G=	ENSP00000331176.7:p.Gln238=
ENST00000332710.8:c.714G=	ENSP00000331791.4:p.Gln238=
ENST00000359500.7:c.714G=	ENSP00000352483.3:p.Gln238=
ENST00000621939.1:c.714G=	ENSP00000477982.1:p.Gln238=
NM_005992.1:c.714G=	NP_005983.1:p.Gln238=
NM_080646.1:c.714G=	NP_542377.1:p.Gln238=
NM_080647.1:c.714G= , LRG_226t1:c.714G=	NP_542378.1:p.Gln238=
XM_006724312.1:c.714G=	XP_006724375.1:p.Gln238=
XM_011530351.1:c.741G=	XP_011528653.1:p.Gln247=
XM_006724312.2:c.714G=	XP_006724375.1:p.Gln238=
XM_017028925.1:c.864G=	XP_016884414.1:p.Gln288=
XM_017028926.1:c.714G=	XP_016884415.1:p.Gln238=
XM_017028927.1:c.15G=	XP_016884416.1:p.Gln5=
XM_017028928.1:c.864G=	XP_016884417.1:p.Gln288=
NM_001379200.1:c.741G= MANE Select	NP_001366129.1:p.Gln247=
NM_080646.2:c.714G=	NP_542377.1:p.Gln238=