Canonical Allele Identifier: CA2396031099

Gene: TBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19764294C= , CM000684.2:g.19764294C=	GRCh38
NC_000022.10:g.19751817C= , CM000684.1:g.19751817C=	GRCh37
NC_000022.9:g.18131817C=	NCBI36
NG_009229.1:g.12592C= , LRG_226:g.12592C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700274.1:c.205C=	ENSP00000514909.1:p.Leu69=
ENST00000649276.2:c.679C= MANE Select	ENSP00000497003.1:p.Leu227=
ENST00000680333.1:c.652C=	ENSP00000505472.1:p.Leu218=
ENST00000329705.11:c.652C=	ENSP00000331176.7:p.Leu218=
ENST00000332710.8:c.652C=	ENSP00000331791.4:p.Leu218=
ENST00000359500.7:c.652C=	ENSP00000352483.3:p.Leu218=
ENST00000621939.1:c.652C=	ENSP00000477982.1:p.Leu218=
NM_005992.1:c.652C=	NP_005983.1:p.Leu218=
NM_080646.1:c.652C=	NP_542377.1:p.Leu218=
NM_080647.1:c.652C= , LRG_226t1:c.652C=	NP_542378.1:p.Leu218=
XM_006724312.1:c.652C=	XP_006724375.1:p.Leu218=
XM_011530351.1:c.679C=	XP_011528653.1:p.Leu227=
XM_006724312.2:c.652C=	XP_006724375.1:p.Leu218=
XM_017028925.1:c.802C=	XP_016884414.1:p.Leu268=
XM_017028926.1:c.652C=	XP_016884415.1:p.Leu218=
XM_017028928.1:c.802C=	XP_016884417.1:p.Leu268=
NM_001379200.1:c.679C= MANE Select	NP_001366129.1:p.Leu227=
NM_080646.2:c.652C=	NP_542377.1:p.Leu218=