Canonical Allele Identifier: CA2396032465

Gene: TBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19766688C= , CM000684.2:g.19766688C=	GRCh38
NC_000022.10:g.19754211C= , CM000684.1:g.19754211C=	GRCh37
NC_000022.9:g.18134211C=	NCBI36
NG_009229.1:g.14986C= , LRG_226:g.14986C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649276.2:c.1336C= MANE Select	ENSP00000497003.1:p.Pro446=
ENST00000329705.11:c.1009+686C=	ENSP00000331176.7:n.1009+686C=
ENST00000332710.8:c.1309C=	ENSP00000331791.4:p.Pro437=
ENST00000359500.7:c.1009+686C=	ENSP00000352483.3:n.1009+686C=
ENST00000621939.1:c.1009+686C=	ENSP00000477982.1:n.1009+686C=
NM_005992.1:c.1009+686C=	NP_005983.1:n.1009+686C=
NM_080646.1:c.1009+686C=	NP_542377.1:n.1009+686C=
NM_080647.1:c.1309C= , LRG_226t1:c.1309C=	NP_542378.1:p.Pro437=
XM_006724312.1:c.1309C=	XP_006724375.1:p.Pro437=
XM_011530351.1:c.1336C=	XP_011528653.1:p.Pro446=
XM_006724312.2:c.1309C=	XP_006724375.1:p.Pro437=
XM_017028925.1:c.1459C=	XP_016884414.1:p.Pro487=
XM_017028926.1:c.1309C=	XP_016884415.1:p.Pro437=
XM_017028927.1:c.664C=	XP_016884416.1:p.Pro222=
XM_017028928.1:c.1159+686C=	XP_016884417.1:n.1159+686C=
NM_001379200.1:c.1336C= MANE Select	NP_001366129.1:p.Pro446=
NM_080646.2:c.1009+686C=	NP_542377.1:n.1009+686C=