Canonical Allele Identifier: CA10102401

Gene: TBX1

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19761194C>T , CM000684.2:g.19761194C>T	GRCh38
NC_000022.10:g.19748717C>T , CM000684.1:g.19748717C>T	GRCh37
NC_000022.9:g.18128717C>T	NCBI36
NG_009229.1:g.9492C>T , LRG_226:g.9492C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001379200.1:c.351C>T MANE Select	NP_001366129.1:p.Ala117=
ENST00000649276.2:c.351C>T MANE Select	ENSP00000497003.1:p.Ala117=
NM_005992.1:c.324C>T	NP_005983.1:p.Ala108=
NM_080646.1:c.324C>T	NP_542377.1:p.Ala108=
NM_080646.2:c.324C>T	NP_542377.1:p.Ala108=
NM_080647.1:c.324C>T , LRG_226t1:c.324C>T	NP_542378.1:p.Ala108=
ENST00000329705.11:c.324C>T	ENSP00000331176.7:p.Ala108=
ENST00000332710.8:c.324C>T	ENSP00000331791.4:p.Ala108=
ENST00000359500.7:c.324C>T	ENSP00000352483.3:p.Ala108=
ENST00000621939.1:c.324C>T	ENSP00000477982.1:p.Ala108=
ENST00000680333.1:c.324C>T	ENSP00000505472.1:p.Ala108=
ENST00000700274.1:c.-38+1517C>T	ENSP00000514909.1:n.-38+1517C>T
XM_006724312.1:c.324C>T	XP_006724375.1:p.Ala108=
XM_006724312.2:c.324C>T	XP_006724375.1:p.Ala108=
XM_011530351.1:c.351C>T	XP_011528653.1:p.Ala117=
XM_017028925.1:c.474C>T	XP_016884414.1:p.Ala158=
XM_017028926.1:c.324C>T	XP_016884415.1:p.Ala108=
XM_017028928.1:c.474C>T	XP_016884417.1:p.Ala158=