Canonical Allele Identifier: CA410683500
Gene: TBX1 HGNC NCBI

Linked Data

dbSNP Id: rs1375795775

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19765083C>G , CM000684.2:g.19765083C>G GRCh38
NC_000022.10:g.19752606C>G , CM000684.1:g.19752606C>G GRCh37
NC_000022.9:g.18132606C>G NCBI36
NG_009229.1:g.13381C>G , LRG_226:g.13381C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700274.1:c.363C>G ENSP00000514909.1:p.Phe121Leu
ENST00000649276.2:c.837C>G MANE Select ENSP00000497003.1:p.Phe279Leu
ENST00000329705.11:c.810C>G ENSP00000331176.7:p.Phe270Leu
ENST00000332710.8:c.810C>G ENSP00000331791.4:p.Phe270Leu
ENST00000359500.7:c.810C>G ENSP00000352483.3:p.Phe270Leu
ENST00000484336.1:n.5C>G
ENST00000621939.1:c.810C>G ENSP00000477982.1:p.Phe270Leu
NM_005992.1:c.810C>G NP_005983.1:p.Phe270Leu
NM_080646.1:c.810C>G NP_542377.1:p.Phe270Leu
NM_080647.1:c.810C>G , LRG_226t1:c.810C>G NP_542378.1:p.Phe270Leu
XM_006724312.1:c.810C>G XP_006724375.1:p.Phe270Leu
XM_011530351.1:c.837C>G XP_011528653.1:p.Phe279Leu
XM_006724312.2:c.810C>G XP_006724375.1:p.Phe270Leu
XM_017028925.1:c.960C>G XP_016884414.1:p.Phe320Leu
XM_017028926.1:c.810C>G XP_016884415.1:p.Phe270Leu
XM_017028927.1:c.111C>G XP_016884416.1:p.Phe37Leu
XM_017028928.1:c.960C>G XP_016884417.1:p.Phe320Leu
NM_001379200.1:c.837C>G MANE Select NP_001366129.1:p.Phe279Leu
NM_080646.2:c.810C>G NP_542377.1:p.Phe270Leu