Canonical Allele Identifier: CA1402950

Gene: RAB3GAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220206020A>T , CM000663.2:g.220206020A>T	GRCh38
NC_000001.10:g.220379362A>T , CM000663.1:g.220379362A>T	GRCh37
NC_000001.9:g.218445985A>T	NCBI36
NG_015837.1:g.71482T>A
NG_015837.2:g.71482T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012414.4:c.613-14T>A MANE Select	NP_036546.2:n.613-14T>A
ENST00000358951.7:c.613-14T>A MANE Select	ENSP00000351832.2:n.613-14T>A
NM_012414.3:c.613-14T>A	NP_036546.2:n.613-14T>A
ENST00000237724.9:n.408-14T>A
ENST00000358951.6:c.613-14T>A	ENSP00000351832.2:n.613-14T>A
ENST00000474178.1:c.*158-14T>A	ENSP00000420156.1:n.*158-14T>A
ENST00000478976.1:n.292-15595T>A
ENST00000484658.1:c.317-14T>A
ENST00000685286.1:c.613-14T>A	ENSP00000509457.1:n.613-14T>A
ENST00000685664.1:c.613-14T>A	ENSP00000509121.1:n.613-14T>A
ENST00000686381.1:c.349-14T>A	ENSP00000509555.1:n.349-14T>A
ENST00000687065.1:c.349-14T>A	ENSP00000510408.1:n.349-14T>A
ENST00000687394.1:n.719-14T>A
ENST00000687647.1:c.349-14T>A	ENSP00000509205.1:n.349-14T>A
ENST00000688035.1:n.1028-14T>A
ENST00000689820.1:c.613-14T>A	ENSP00000509387.1:n.613-14T>A
ENST00000690315.1:c.613-14T>A	ENSP00000509834.1:n.613-14T>A
ENST00000690373.1:n.952-14T>A
ENST00000690379.1:n.643-14T>A
ENST00000690824.1:c.613-14T>A	ENSP00000510709.1:n.613-14T>A
ENST00000691661.1:c.625-14T>A	ENSP00000510185.1:n.625-14T>A
ENST00000691862.1:c.511-14T>A	ENSP00000509291.1:n.511-14T>A
ENST00000692813.1:c.613-14T>A	ENSP00000509080.1:n.613-14T>A
ENST00000692972.1:c.613-14T>A	ENSP00000510753.1:n.613-14T>A
ENST00000693602.1:n.706-14T>A