Canonical Allele Identifier: CA2650564399

Gene: RAB3GAP2

Linked Data

• gnomAD v4: 1-220191373-TGGGGGTGG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220191376_220191383del , CM000663.2:g.220191376_220191383del	GRCh38
NC_000001.10:g.220364718_220364725del , CM000663.1:g.220364718_220364725del	GRCh37
NC_000001.9:g.218431341_218431348del	NCBI36
NG_015837.1:g.86121_86128del
NG_015837.2:g.86121_86128del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685286.1:c.1271-97_1271-90del	ENSP00000509457.1:n.1271-97_1271-90del
ENST00000685664.1:c.1271-97_1271-90del	ENSP00000509121.1:n.1271-97_1271-90del
ENST00000686381.1:c.1007-97_1007-90del	ENSP00000509555.1:n.1007-97_1007-90del
ENST00000687065.1:c.1007-97_1007-90del	ENSP00000510408.1:n.1007-97_1007-90del
ENST00000687394.1:n.1377-97_1377-90del
ENST00000687647.1:c.1007-97_1007-90del	ENSP00000509205.1:n.1007-97_1007-90del
ENST00000688035.1:n.1686-97_1686-90del
ENST00000690315.1:c.1172-97_1172-90del	ENSP00000509834.1:n.1172-97_1172-90del
ENST00000690373.1:n.1610-97_1610-90del
ENST00000690379.1:n.1301-97_1301-90del
ENST00000690824.1:c.1271-97_1271-90del	ENSP00000510709.1:n.1271-97_1271-90del
ENST00000691661.1:c.1283-97_1283-90del	ENSP00000510185.1:n.1283-97_1283-90del
ENST00000691862.1:c.1169-97_1169-90del	ENSP00000509291.1:n.1169-97_1169-90del
ENST00000692813.1:c.1271-97_1271-90del	ENSP00000509080.1:n.1271-97_1271-90del
ENST00000692972.1:c.1346-97_1346-90del	ENSP00000510753.1:n.1346-97_1346-90del
ENST00000693454.1:n.481-97_481-90del
ENST00000693602.1:n.1364-97_1364-90del
ENST00000358951.7:c.1271-97_1271-90del MANE Select	ENSP00000351832.2:n.1271-97_1271-90del
ENST00000358951.6:c.1271-97_1271-90del	ENSP00000351832.2:n.1271-97_1271-90del
ENST00000478976.1:n.292-956_292-949del
NM_012414.3:c.1271-97_1271-90del	NP_036546.2:n.1271-97_1271-90del
NM_012414.4:c.1271-97_1271-90del MANE Select	NP_036546.2:n.1271-97_1271-90del