Canonical Allele Identifier: CA11023080
Gene: TGFBRAP1 HGNC NCBI

Linked Data

dbSNP Id: rs1030877

Genomic Alleles

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

Transcript Alleles

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