Canonical Allele Identifier: CA2243599763

Gene: RAP1GAP2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_015085.5:c.81-37066C= MANE Select	NP_055900.4:n.81-37066C=
ENST00000254695.13:c.81-37066C= MANE Select	ENSP00000254695.8:n.81-37066C=
NM_001100398.1:c.81-37066C=	NP_001093868.1:n.81-37066C=
NM_001100398.2:c.81-37066C=	NP_001093868.1:n.81-37066C=
NM_001330058.1:c.24-37066C=	NP_001316987.1:n.24-37066C=
NM_001330058.2:c.24-37066C=	NP_001316987.1:n.24-37066C=
NM_015085.4:c.81-37066C=	NP_055900.4:n.81-37066C=
ENST00000254695.12:c.81-37066C=	ENSP00000254695.8:n.81-37066C=
ENST00000366401.8:c.81-37066C=	ENSP00000389824.2:n.81-37066C=
ENST00000540393.6:c.24-37066C=	ENSP00000439688.2:n.24-37066C=
ENST00000542807.1:c.81-37066C=	ENSP00000444890.1:n.81-37066C=
ENST00000637138.1:c.204-37066C=	ENSP00000490321.1:n.204-37066C=
ENST00000697391.1:c.107+14116C=	ENSP00000513294.1:n.107+14116C=
XM_005256541.1:c.117-37066C=	XP_005256598.1:n.117-37066C=
XM_005256542.2:c.107+14116C=	XP_005256599.1:n.107+14116C=
XM_006721477.2:c.24-37066C=	XP_006721540.1:n.24-37066C=
XM_011523738.1:c.204-37066C=	XP_011522040.1:n.204-37066C=
XM_011523738.2:c.204-37066C=	XP_011522040.1:n.204-37066C=
XM_011523739.1:c.204-37066C=	XP_011522041.1:n.204-37066C=
XM_011523739.2:c.204-37066C=	XP_011522041.1:n.204-37066C=
XM_011523740.1:c.69-37066C=	XP_011522042.1:n.69-37066C=
XM_011523741.1:c.24-37066C=	XP_011522043.1:n.24-37066C=
XM_011523741.2:c.24-37066C=	XP_011522043.1:n.24-37066C=
XM_017024371.1:c.54-37066C=	XP_016879860.1:n.54-37066C=
XM_024450659.1:c.204-37066C=	XP_024306427.1:n.204-37066C=