Canonical Allele Identifier: CA11023069

Gene: TGFBRAP1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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