Canonical Allele Identifier: CA14501195
Gene: RAP1GAP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.2868218C>T , CM000679.2:g.2868218C>T GRCh38
NC_000017.10:g.2771512C>T , CM000679.1:g.2771512C>T GRCh37
NC_000017.9:g.2718262C>T NCBI36
NG_013030.1:g.76781C>T
NG_013030.2:g.117521C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697391.1:c.107+14116C>T ENSP00000513294.1:n.107+14116C>T
ENST00000254695.13:c.81-37066C>T MANE Select ENSP00000254695.8:n.81-37066C>T
ENST00000637138.1:c.204-37066C>T ENSP00000490321.1:n.204-37066C>T
ENST00000254695.12:c.81-37066C>T ENSP00000254695.8:n.81-37066C>T
ENST00000366401.8:c.81-37066C>T ENSP00000389824.2:n.81-37066C>T
ENST00000540393.6:c.24-37066C>T ENSP00000439688.2:n.24-37066C>T
ENST00000542807.1:c.81-37066C>T ENSP00000444890.1:n.81-37066C>T
NM_001100398.1:c.81-37066C>T NP_001093868.1:n.81-37066C>T
NM_015085.4:c.81-37066C>T NP_055900.4:n.81-37066C>T
XM_005256541.1:c.117-37066C>T XP_005256598.1:n.117-37066C>T
XM_005256542.2:c.107+14116C>T XP_005256599.1:n.107+14116C>T
XM_006721477.2:c.24-37066C>T XP_006721540.1:n.24-37066C>T
XM_011523738.1:c.204-37066C>T XP_011522040.1:n.204-37066C>T
XM_011523739.1:c.204-37066C>T XP_011522041.1:n.204-37066C>T
XM_011523740.1:c.69-37066C>T XP_011522042.1:n.69-37066C>T
XM_011523741.1:c.24-37066C>T XP_011522043.1:n.24-37066C>T
NM_001330058.1:c.24-37066C>T NP_001316987.1:n.24-37066C>T
XM_011523738.2:c.204-37066C>T XP_011522040.1:n.204-37066C>T
XM_011523739.2:c.204-37066C>T XP_011522041.1:n.204-37066C>T
XM_011523741.2:c.24-37066C>T XP_011522043.1:n.24-37066C>T
XM_017024371.1:c.54-37066C>T XP_016879860.1:n.54-37066C>T
XM_024450659.1:c.204-37066C>T XP_024306427.1:n.204-37066C>T
NM_015085.5:c.81-37066C>T MANE Select NP_055900.4:n.81-37066C>T
NM_001100398.2:c.81-37066C>T NP_001093868.1:n.81-37066C>T
NM_001330058.2:c.24-37066C>T NP_001316987.1:n.24-37066C>T
Search 100 bp 5'
Search 100 bp 3'