Canonical Allele Identifier: CA1276636187

Gene: TGFBRAP1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.105294056G= , CM000664.2:g.105294056G=	GRCh38
NC_000002.11:g.105910513G= , CM000664.1:g.105910513G=	GRCh37
NC_000002.10:g.105276945G=	NCBI36
NG_050952.1:g.40659C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393359.7:c.1038+2300C= MANE Select	ENSP00000377027.2:n.1038+2300C=
ENST00000258449.2:c.1038+2300C=	ENSP00000258449.1:n.1038+2300C=
ENST00000393359.6:c.1038+2300C=	ENSP00000377027.2:n.1038+2300C=
ENST00000595531.5:c.1038+2300C=	ENSP00000471434.2:n.1038+2300C=
NM_001142621.2:c.1038+2300C=	NP_001136093.1:n.1038+2300C=
NM_004257.5:c.1038+2300C=	NP_004248.2:n.1038+2300C=
XM_011512193.1:c.1038+2300C=	XP_011510495.1:n.1038+2300C=
NM_001328646.1:c.1038+2300C=	NP_001315575.1:n.1038+2300C=
NR_137328.1:n.1087+2300C=
XM_017005339.2:c.-242+2300C=	XP_016860828.1:n.-242+2300C=
NM_004257.6:c.1038+2300C= MANE Select	NP_004248.2:n.1038+2300C=
NM_001142621.3:c.1038+2300C=	NP_001136093.1:n.1038+2300C=
NM_001328646.2:c.1038+2300C=	NP_001315575.1:n.1038+2300C=
NM_001328646.3:c.1038+2300C=	NP_001315575.1:n.1038+2300C=
NR_137328.2:n.1166+2300C=