Canonical Allele Identifier: CA2396032626

Gene: TBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19766887C= , CM000684.2:g.19766887C=	GRCh38
NC_000022.10:g.19754410C= , CM000684.1:g.19754410C=	GRCh37
NC_000022.9:g.18134410C=	NCBI36
NG_009229.1:g.15185C= , LRG_226:g.15185C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649276.2:c.*20C= MANE Select	ENSP00000497003.1:n.*20C=
ENST00000329705.11:c.1009+885C=	ENSP00000331176.7:n.1009+885C=
ENST00000332710.8:c.*20C=	ENSP00000331791.4:n.*20C=
ENST00000359500.7:c.1009+885C=	ENSP00000352483.3:n.1009+885C=
ENST00000621939.1:c.1009+885C=	ENSP00000477982.1:n.1009+885C=
NM_005992.1:c.1009+885C=	NP_005983.1:n.1009+885C=
NM_080646.1:c.1009+885C=	NP_542377.1:n.1009+885C=
NM_080647.1:c.*20C= , LRG_226t1:c.*20C=	NP_542378.1:n.*20C=
XM_006724312.1:c.*20C=	XP_006724375.1:n.*20C=
XM_011530351.1:c.*20C=	XP_011528653.1:n.*20C=
XM_006724312.2:c.*20C=	XP_006724375.1:n.*20C=
XM_017028925.1:c.*20C=	XP_016884414.1:n.*20C=
XM_017028926.1:c.*20C=	XP_016884415.1:n.*20C=
XM_017028927.1:c.*20C=	XP_016884416.1:n.*20C=
XM_017028928.1:c.1159+885C=	XP_016884417.1:n.1159+885C=
NM_001379200.1:c.*20C= MANE Select	NP_001366129.1:n.*20C=
NM_080646.2:c.1009+885C=	NP_542377.1:n.1009+885C=