Canonical Allele Identifier: CA10102573
Gene: TBX1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.382C>A ENSP00000514909.1:p.Gln128Lys
ENST00000649276.2:c.856C>A MANE Select ENSP00000497003.1:p.Gln286Lys
ENST00000329705.11:c.829C>A ENSP00000331176.7:p.Gln277Lys
ENST00000332710.8:c.829C>A ENSP00000331791.4:p.Gln277Lys
ENST00000359500.7:c.829C>A ENSP00000352483.3:p.Gln277Lys
ENST00000484336.1:n.24C>A
ENST00000621939.1:c.829C>A ENSP00000477982.1:p.Gln277Lys
NM_005992.1:c.829C>A NP_005983.1:p.Gln277Lys
NM_080646.1:c.829C>A NP_542377.1:p.Gln277Lys
NM_080647.1:c.829C>A , LRG_226t1:c.829C>A NP_542378.1:p.Gln277Lys
XM_006724312.1:c.829C>A XP_006724375.1:p.Gln277Lys
XM_011530351.1:c.856C>A XP_011528653.1:p.Gln286Lys
XM_006724312.2:c.829C>A XP_006724375.1:p.Gln277Lys
XM_017028925.1:c.979C>A XP_016884414.1:p.Gln327Lys
XM_017028926.1:c.829C>A XP_016884415.1:p.Gln277Lys
XM_017028927.1:c.130C>A XP_016884416.1:p.Gln44Lys
XM_017028928.1:c.979C>A XP_016884417.1:p.Gln327Lys
NM_001379200.1:c.856C>A MANE Select NP_001366129.1:p.Gln286Lys
NM_080646.2:c.829C>A NP_542377.1:p.Gln277Lys