Canonical Allele Identifier: CA1222316014

Gene: RAB3GAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220202376T= , CM000663.2:g.220202376T=	GRCh38
NC_000001.10:g.220375718T= , CM000663.1:g.220375718T=	GRCh37
NC_000001.9:g.218442341T=	NCBI36
NG_015837.1:g.75126A=
NG_015837.2:g.75126A=

Transcript Alleles

HGVS	Amino-acid Change
NM_012414.4:c.713-2A= MANE Select	NP_036546.2:n.713-2A=
ENST00000358951.7:c.713-2A= MANE Select	ENSP00000351832.2:n.713-2A=
NM_012414.3:c.713-2A=	NP_036546.2:n.713-2A=
ENST00000237724.9:n.508-2A=
ENST00000358951.6:c.713-2A=	ENSP00000351832.2:n.713-2A=
ENST00000478976.1:n.292-11951A=
ENST00000484658.1:c.417-2A=
ENST00000685286.1:c.713-2A=	ENSP00000509457.1:n.713-2A=
ENST00000685664.1:c.713-2A=	ENSP00000509121.1:n.713-2A=
ENST00000686381.1:c.449-2A=	ENSP00000509555.1:n.449-2A=
ENST00000687065.1:c.449-2A=	ENSP00000510408.1:n.449-2A=
ENST00000687394.1:n.819-2A=
ENST00000687647.1:c.449-2A=	ENSP00000509205.1:n.449-2A=
ENST00000688035.1:n.1128-2A=
ENST00000689820.1:c.713-2A=	ENSP00000509387.1:n.713-2A=
ENST00000690315.1:c.712+3531A=	ENSP00000509834.1:n.712+3531A=
ENST00000690373.1:n.1052-2A=
ENST00000690379.1:n.743-2A=
ENST00000690824.1:c.713-2A=	ENSP00000510709.1:n.713-2A=
ENST00000691661.1:c.725-2A=	ENSP00000510185.1:n.725-2A=
ENST00000691862.1:c.611-2A=	ENSP00000509291.1:n.611-2A=
ENST00000692813.1:c.713-2A=	ENSP00000509080.1:n.713-2A=
ENST00000692972.1:c.713-2A=	ENSP00000510753.1:n.713-2A=
ENST00000693602.1:n.806-2A=