Canonical Allele Identifier: CA1141842474

Gene: RAB3GAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220191283C= , CM000663.2:g.220191283C=	GRCh38
NC_000001.10:g.220364625C= , CM000663.1:g.220364625C=	GRCh37
NC_000001.9:g.218431248C=	NCBI36
NG_015837.1:g.86219G=
NG_015837.2:g.86219G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685286.1:c.1272G=	ENSP00000509457.1:p.Gly424=
ENST00000685664.1:c.1272G=	ENSP00000509121.1:p.Gly424=
ENST00000686381.1:c.1008G=	ENSP00000509555.1:p.Gly336=
ENST00000687065.1:c.1008G=	ENSP00000510408.1:p.Gly336=
ENST00000687394.1:n.1378G=
ENST00000687647.1:c.1008G=	ENSP00000509205.1:p.Gly336=
ENST00000688035.1:n.1687G=
ENST00000690315.1:c.1173G=	ENSP00000509834.1:p.Gly391=
ENST00000690373.1:n.1611G=
ENST00000690379.1:n.1302G=
ENST00000690824.1:c.1272G=	ENSP00000510709.1:p.Gly424=
ENST00000691661.1:c.1284G=	ENSP00000510185.1:p.Gly428=
ENST00000691862.1:c.1170G=	ENSP00000509291.1:p.Gly390=
ENST00000692813.1:c.1272G=	ENSP00000509080.1:p.Gly424=
ENST00000692972.1:c.1347G=	ENSP00000510753.1:p.Gly449=
ENST00000693454.1:n.482G=
ENST00000693602.1:n.1365G=
ENST00000358951.7:c.1272G= MANE Select	ENSP00000351832.2:p.Gly424=
ENST00000358951.6:c.1272G=	ENSP00000351832.2:p.Gly424=
ENST00000478976.1:n.292-858G=
NM_012414.3:c.1272G=	NP_036546.2:p.Gly424=
NM_012414.4:c.1272G= MANE Select	NP_036546.2:p.Gly424=