Canonical Allele Identifier: CA410683779
Community Standard Title: NM_001379200.1(TBX1):c.955G>C (p.Gly319Arg)
Gene: TBX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.19765921G>C , CM000684.2:g.19765921G>C GRCh38
NC_000022.10:g.19753444G>C , CM000684.1:g.19753444G>C GRCh37
NC_000022.9:g.18133444G>C NCBI36
NG_009229.1:g.14219G>C , LRG_226:g.14219G>C

Transcript Alleles

HGVS Amino-acid Change
NM_001379200.1:c.955G>C MANE Select NP_001366129.1:p.Gly319Arg
ENST00000649276.2:c.955G>C MANE Select ENSP00000497003.1:p.Gly319Arg
NM_005992.1:c.928G>C NP_005983.1:p.Gly310Arg
NM_080646.1:c.928G>C NP_542377.1:p.Gly310Arg
NM_080646.2:c.928G>C NP_542377.1:p.Gly310Arg
NM_080647.1:c.928G>C , LRG_226t1:c.928G>C NP_542378.1:p.Gly310Arg
ENST00000329705.11:c.928G>C ENSP00000331176.7:p.Gly310Arg
ENST00000332710.8:c.928G>C ENSP00000331791.4:p.Gly310Arg
ENST00000359500.7:c.928G>C ENSP00000352483.3:p.Gly310Arg
ENST00000484336.1:n.123G>C
ENST00000621939.1:c.928G>C ENSP00000477982.1:p.Gly310Arg
ENST00000700274.1:c.481G>C ENSP00000514909.1:p.Gly161Arg
XM_006724312.1:c.928G>C XP_006724375.1:p.Gly310Arg
XM_006724312.2:c.928G>C XP_006724375.1:p.Gly310Arg
XM_011530351.1:c.955G>C XP_011528653.1:p.Gly319Arg
XM_017028925.1:c.1078G>C XP_016884414.1:p.Gly360Arg
XM_017028926.1:c.928G>C XP_016884415.1:p.Gly310Arg
XM_017028927.1:c.283G>C XP_016884416.1:p.Gly95Arg
XM_017028928.1:c.1078G>C XP_016884417.1:p.Gly360Arg