Canonical Allele Identifier: CA423262131

Gene: RAB3GAP2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220167560A>T , CM000663.2:g.220167560A>T	GRCh38
NC_000001.10:g.220340902A>T , CM000663.1:g.220340902A>T	GRCh37
NC_000001.9:g.218407525A>T	NCBI36
NG_015837.1:g.109942T>A
NG_015837.2:g.109942T>A

Transcript Alleles

HGVS	Amino-acid Change
NM_012414.4:c.2922T>A MANE Select	NP_036546.2:p.Gly974=
ENST00000358951.7:c.2922T>A MANE Select	ENSP00000351832.2:p.Gly974=
NM_012414.3:c.2922T>A	NP_036546.2:p.Gly974=
ENST00000358951.6:c.2922T>A	ENSP00000351832.2:p.Gly974=
ENST00000685286.1:c.*251T>A	ENSP00000509457.1:n.*251T>A
ENST00000685664.1:c.2922T>A	ENSP00000509121.1:p.Gly974=
ENST00000686381.1:c.2658T>A	ENSP00000509555.1:p.Gly886=
ENST00000687065.1:c.2658T>A	ENSP00000510408.1:p.Gly886=
ENST00000687394.1:n.3028T>A
ENST00000687647.1:c.2658T>A	ENSP00000509205.1:p.Gly886=
ENST00000688035.1:n.3337T>A
ENST00000690315.1:c.2823T>A	ENSP00000509834.1:p.Gly941=
ENST00000690373.1:n.3261T>A
ENST00000690824.1:c.2922T>A	ENSP00000510709.1:p.Gly974=
ENST00000691661.1:c.2934T>A	ENSP00000510185.1:p.Gly978=
ENST00000691862.1:c.2820T>A	ENSP00000509291.1:p.Gly940=
ENST00000692813.1:c.2922T>A	ENSP00000509080.1:p.Gly974=
ENST00000692972.1:c.2997T>A	ENSP00000510753.1:p.Gly999=
ENST00000693602.1:n.3015T>A