Canonical Allele Identifier: CA8001630
Community Standard Title: NM_004608.4(TBX6):c.1227G>A (p.Pro409=)
Gene: TBX6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30086309C>T , CM000678.2:g.30086309C>T GRCh38
NC_000016.9:g.30097630C>T , CM000678.1:g.30097630C>T GRCh37
NC_000016.8:g.30005131C>T NCBI36
NG_023283.1:g.10576G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004608.4:c.1227G>A MANE Select NP_004599.2:p.Pro409=
ENST00000395224.7:c.1227G>A MANE Select ENSP00000378650.2:p.Pro409=
NM_004608.3:c.1227G>A NP_004599.2:p.Pro409=
ENST00000279386.6:c.1227G>A ENSP00000279386.2:p.Pro409=
ENST00000395224.6:c.1227G>A ENSP00000378650.2:p.Pro409=
ENST00000567664.5:c.*361G>A ENSP00000460425.1:n.*361G>A
ENST00000627355.2:c.1227G>A ENSP00000485762.1:p.Pro409=
XM_005255523.1:c.1227G>A XP_005255580.1:p.Pro409=
XM_005255523.2:c.1227G>A XP_005255580.1:p.Pro409=
XM_011545926.1:c.1227G>A XP_011544228.1:p.Pro409=
XM_011545926.3:c.1227G>A XP_011544228.1:p.Pro409=
XM_017023614.1:c.1227G>A XP_016879103.1:p.Pro409=