Canonical Allele Identifier: CA2650564376
Gene: RAB3GAP2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220191347_220191348insGAGCCCATCTCAAAAAAATAA , CM000663.2:g.220191347_220191348insGAGCCCATCTCAAAAAAATAA GRCh38
NC_000001.10:g.220364689_220364690insGAGCCCATCTCAAAAAAATAA , CM000663.1:g.220364689_220364690insGAGCCCATCTCAAAAAAATAA GRCh37
NC_000001.9:g.218431312_218431313insGAGCCCATCTCAAAAAAATAA NCBI36
NG_015837.1:g.86154_86155insTTATTTTTTTGAGATGGGCTC
NG_015837.2:g.86154_86155insTTATTTTTTTGAGATGGGCTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000685286.1:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC ENSP00000509457.1:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC
ENST00000685664.1:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC ENSP00000509121.1:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC
ENST00000686381.1:c.1007-64_1007-63insTTATTTTTTTGAGATGGGCTC ENSP00000509555.1:n.1007-64_1007-63insTTATTTTTTTGAGATGGGCTC
ENST00000687065.1:c.1007-64_1007-63insTTATTTTTTTGAGATGGGCTC ENSP00000510408.1:n.1007-64_1007-63insTTATTTTTTTGAGATGGGCTC
ENST00000687394.1:n.1377-64_1377-63insTTATTTTTTTGAGATGGGCTC
ENST00000687647.1:c.1007-64_1007-63insTTATTTTTTTGAGATGGGCTC ENSP00000509205.1:n.1007-64_1007-63insTTATTTTTTTGAGATGGGCTC
ENST00000688035.1:n.1686-64_1686-63insTTATTTTTTTGAGATGGGCTC
ENST00000690315.1:c.1172-64_1172-63insTTATTTTTTTGAGATGGGCTC ENSP00000509834.1:n.1172-64_1172-63insTTATTTTTTTGAGATGGGCTC
ENST00000690373.1:n.1610-64_1610-63insTTATTTTTTTGAGATGGGCTC
ENST00000690379.1:n.1301-64_1301-63insTTATTTTTTTGAGATGGGCTC
ENST00000690824.1:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC ENSP00000510709.1:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC
ENST00000691661.1:c.1283-64_1283-63insTTATTTTTTTGAGATGGGCTC ENSP00000510185.1:n.1283-64_1283-63insTTATTTTTTTGAGATGGGCTC
ENST00000691862.1:c.1169-64_1169-63insTTATTTTTTTGAGATGGGCTC ENSP00000509291.1:n.1169-64_1169-63insTTATTTTTTTGAGATGGGCTC
ENST00000692813.1:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC ENSP00000509080.1:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC
ENST00000692972.1:c.1346-64_1346-63insTTATTTTTTTGAGATGGGCTC ENSP00000510753.1:n.1346-64_1346-63insTTATTTTTTTGAGATGGGCTC
ENST00000693454.1:n.481-64_481-63insTTATTTTTTTGAGATGGGCTC
ENST00000693602.1:n.1364-64_1364-63insTTATTTTTTTGAGATGGGCTC
ENST00000358951.7:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC MANE Select ENSP00000351832.2:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC
ENST00000358951.6:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC ENSP00000351832.2:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC
ENST00000478976.1:n.292-923_292-922insTTATTTTTTTGAGATGGGCTC
NM_012414.3:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC NP_036546.2:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC
NM_012414.4:c.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC MANE Select NP_036546.2:n.1271-64_1271-63insTTATTTTTTTGAGATGGGCTC