Canonical Allele Identifier: CA410683537

Gene: TBX1

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.19765102C>T , CM000684.2:g.19765102C>T	GRCh38
NC_000022.10:g.19752625C>T , CM000684.1:g.19752625C>T	GRCh37
NC_000022.9:g.18132625C>T	NCBI36
NG_009229.1:g.13400C>T , LRG_226:g.13400C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700274.1:c.382C>T	ENSP00000514909.1:p.Gln128Ter
ENST00000649276.2:c.856C>T MANE Select	ENSP00000497003.1:p.Gln286Ter
ENST00000329705.11:c.829C>T	ENSP00000331176.7:p.Gln277Ter
ENST00000332710.8:c.829C>T	ENSP00000331791.4:p.Gln277Ter
ENST00000359500.7:c.829C>T	ENSP00000352483.3:p.Gln277Ter
ENST00000484336.1:n.24C>T
ENST00000621939.1:c.829C>T	ENSP00000477982.1:p.Gln277Ter
NM_005992.1:c.829C>T	NP_005983.1:p.Gln277Ter
NM_080646.1:c.829C>T	NP_542377.1:p.Gln277Ter
NM_080647.1:c.829C>T , LRG_226t1:c.829C>T	NP_542378.1:p.Gln277Ter
XM_006724312.1:c.829C>T	XP_006724375.1:p.Gln277Ter
XM_011530351.1:c.856C>T	XP_011528653.1:p.Gln286Ter
XM_006724312.2:c.829C>T	XP_006724375.1:p.Gln277Ter
XM_017028925.1:c.979C>T	XP_016884414.1:p.Gln327Ter
XM_017028926.1:c.829C>T	XP_016884415.1:p.Gln277Ter
XM_017028927.1:c.130C>T	XP_016884416.1:p.Gln44Ter
XM_017028928.1:c.979C>T	XP_016884417.1:p.Gln327Ter
NM_001379200.1:c.856C>T MANE Select	NP_001366129.1:p.Gln286Ter
NM_080646.2:c.829C>T	NP_542377.1:p.Gln277Ter