Canonical Allele Identifier: CA2396032505

Gene: TBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19766740A= , CM000684.2:g.19766740A=	GRCh38
NC_000022.10:g.19754263A= , CM000684.1:g.19754263A=	GRCh37
NC_000022.9:g.18134263A=	NCBI36
NG_009229.1:g.15038A= , LRG_226:g.15038A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000649276.2:c.1388A= MANE Select	ENSP00000497003.1:p.His463=
ENST00000329705.11:c.1009+738A=	ENSP00000331176.7:n.1009+738A=
ENST00000332710.8:c.1361A=	ENSP00000331791.4:p.His454=
ENST00000359500.7:c.1009+738A=	ENSP00000352483.3:n.1009+738A=
ENST00000621939.1:c.1009+738A=	ENSP00000477982.1:n.1009+738A=
NM_005992.1:c.1009+738A=	NP_005983.1:n.1009+738A=
NM_080646.1:c.1009+738A=	NP_542377.1:n.1009+738A=
NM_080647.1:c.1361A= , LRG_226t1:c.1361A=	NP_542378.1:p.His454=
XM_006724312.1:c.1361A=	XP_006724375.1:p.His454=
XM_011530351.1:c.1388A=	XP_011528653.1:p.His463=
XM_006724312.2:c.1361A=	XP_006724375.1:p.His454=
XM_017028925.1:c.1511A=	XP_016884414.1:p.His504=
XM_017028926.1:c.1361A=	XP_016884415.1:p.His454=
XM_017028927.1:c.716A=	XP_016884416.1:p.His239=
XM_017028928.1:c.1159+738A=	XP_016884417.1:n.1159+738A=
NM_001379200.1:c.1388A= MANE Select	NP_001366129.1:p.His463=
NM_080646.2:c.1009+738A=	NP_542377.1:n.1009+738A=