Canonical Allele Identifier: CA1276630649

Gene: TGFBRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.105281283T= , CM000664.2:g.105281283T=	GRCh38
NC_000002.11:g.105897740T= , CM000664.1:g.105897740T=	GRCh37
NC_000002.10:g.105264172T=	NCBI36
NG_050952.1:g.53432A=

Transcript Alleles

HGVS	Amino-acid Change
NM_004257.6:c.1122-560A= MANE Select	NP_004248.2:n.1122-560A=
ENST00000393359.7:c.1122-560A= MANE Select	ENSP00000377027.2:n.1122-560A=
NM_001142621.2:c.1122-560A=	NP_001136093.1:n.1122-560A=
NM_001142621.3:c.1122-560A=	NP_001136093.1:n.1122-560A=
NM_001328646.1:c.1122-560A=	NP_001315575.1:n.1122-560A=
NM_001328646.2:c.1122-560A=	NP_001315575.1:n.1122-560A=
NM_001328646.3:c.1122-560A=	NP_001315575.1:n.1122-560A=
NM_004257.5:c.1122-560A=	NP_004248.2:n.1122-560A=
NR_137328.1:n.1171-560A=
NR_137328.2:n.1250-560A=
ENST00000258449.2:c.1122-560A=	ENSP00000258449.1:n.1122-560A=
ENST00000393359.6:c.1122-560A=	ENSP00000377027.2:n.1122-560A=
ENST00000595531.5:c.1122-560A=	ENSP00000471434.2:n.1122-560A=
XM_011512193.1:c.1122-560A=	XP_011510495.1:n.1122-560A=
XM_017005339.2:c.-158-541A=	XP_016860828.1:n.-158-541A=