Canonical Allele Identifier: CA410685161

Gene: TBX1

Linked Data

• MyVariant Identifiers: chr22:g.19754244C>A (hg19) ; chr22:g.19766721C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19766721C>A , CM000684.2:g.19766721C>A	GRCh38
NC_000022.10:g.19754244C>A , CM000684.1:g.19754244C>A	GRCh37
NC_000022.9:g.18134244C>A	NCBI36
NG_009229.1:g.15019C>A , LRG_226:g.15019C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000649276.2:c.1369C>A MANE Select	ENSP00000497003.1:p.Pro457Thr
ENST00000329705.11:c.1009+719C>A	ENSP00000331176.7:n.1009+719C>A
ENST00000332710.8:c.1342C>A	ENSP00000331791.4:p.Pro448Thr
ENST00000359500.7:c.1009+719C>A	ENSP00000352483.3:n.1009+719C>A
ENST00000621939.1:c.1009+719C>A	ENSP00000477982.1:n.1009+719C>A
NM_005992.1:c.1009+719C>A	NP_005983.1:n.1009+719C>A
NM_080646.1:c.1009+719C>A	NP_542377.1:n.1009+719C>A
NM_080647.1:c.1342C>A , LRG_226t1:c.1342C>A	NP_542378.1:p.Pro448Thr
XM_006724312.1:c.1342C>A	XP_006724375.1:p.Pro448Thr
XM_011530351.1:c.1369C>A	XP_011528653.1:p.Pro457Thr
XM_006724312.2:c.1342C>A	XP_006724375.1:p.Pro448Thr
XM_017028925.1:c.1492C>A	XP_016884414.1:p.Pro498Thr
XM_017028926.1:c.1342C>A	XP_016884415.1:p.Pro448Thr
XM_017028927.1:c.697C>A	XP_016884416.1:p.Pro233Thr
XM_017028928.1:c.1159+719C>A	XP_016884417.1:n.1159+719C>A
NM_001379200.1:c.1369C>A MANE Select	NP_001366129.1:p.Pro457Thr
NM_080646.2:c.1009+719C>A	NP_542377.1:n.1009+719C>A