Canonical Allele Identifier: CA1140724096

Gene: TBX15

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.118884844A= , CM000663.2:g.118884844A=	GRCh38
NC_000001.10:g.119427467A= , CM000663.1:g.119427467A=	GRCh37
NC_000001.9:g.119228990A=	NCBI36
NG_013361.1:g.109713T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369429.5:c.1697T= MANE Select	ENSP00000358437.3:p.Met566=
ENST00000207157.7:c.1379T=	ENSP00000207157.3:p.Met460=
ENST00000369429.3:c.1697T=	ENSP00000358437.3:p.Met566=
ENST00000449873.5:c.881T=	ENSP00000398625.1:p.Met294=
NM_152380.2:c.1379T=	NP_689593.2:p.Met460=
XM_005271161.2:c.1796T=	XP_005271218.1:p.Met599=
XM_005271162.1:c.1697T=	XP_005271219.1:p.Met566=
XM_011542052.1:c.851T=	XP_011540354.1:p.Met284=
NM_001330677.1:c.1697T=	NP_001317606.1:p.Met566=
XM_005271161.4:c.1796T=	XP_005271218.1:p.Met599=
XM_011542052.2:c.851T=	XP_011540354.1:p.Met284=
NM_001330677.2:c.1697T= MANE Select	NP_001317606.1:p.Met566=
NM_152380.3:c.1379T=	NP_689593.2:p.Met460=