Canonical Allele Identifier: CA423169597

Gene: RAB3GAP2

Linked Data

• MyVariant Identifiers: chr1:g.220364568C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220191226C>G , CM000663.2:g.220191226C>G	GRCh38
NC_000001.10:g.220364568C>G , CM000663.1:g.220364568C>G	GRCh37
NC_000001.9:g.218431191C>G	NCBI36
NG_015837.1:g.86276G>C
NG_015837.2:g.86276G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685286.1:c.1329G>C	ENSP00000509457.1:p.Val443=
ENST00000685664.1:c.1329G>C	ENSP00000509121.1:p.Val443=
ENST00000686381.1:c.1065G>C	ENSP00000509555.1:p.Val355=
ENST00000687065.1:c.1065G>C	ENSP00000510408.1:p.Val355=
ENST00000687394.1:n.1435G>C
ENST00000687647.1:c.1065G>C	ENSP00000509205.1:p.Val355=
ENST00000688035.1:n.1744G>C
ENST00000690315.1:c.1230G>C	ENSP00000509834.1:p.Val410=
ENST00000690373.1:n.1668G>C
ENST00000690379.1:n.1359G>C
ENST00000690824.1:c.1329G>C	ENSP00000510709.1:p.Val443=
ENST00000691661.1:c.1341G>C	ENSP00000510185.1:p.Val447=
ENST00000691862.1:c.1227G>C	ENSP00000509291.1:p.Val409=
ENST00000692813.1:c.1329G>C	ENSP00000509080.1:p.Val443=
ENST00000692972.1:c.1404G>C	ENSP00000510753.1:p.Val468=
ENST00000693454.1:n.539G>C
ENST00000693602.1:n.1422G>C
ENST00000358951.7:c.1329G>C MANE Select	ENSP00000351832.2:p.Val443=
ENST00000358951.6:c.1329G>C	ENSP00000351832.2:p.Val443=
ENST00000478976.1:n.292-801G>C
NM_012414.3:c.1329G>C	NP_036546.2:p.Val443=
NM_012414.4:c.1329G>C MANE Select	NP_036546.2:p.Val443=