Canonical Allele Identifier: CA2747830115
Gene: RAB3GAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.220191378dup , CM000663.2:g.220191378dup GRCh38
NC_000001.10:g.220364720dup , CM000663.1:g.220364720dup GRCh37
NC_000001.9:g.218431343dup NCBI36
NG_015837.1:g.86128dup
NG_015837.2:g.86128dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000685286.1:c.1271-90dup ENSP00000509457.1:n.1271-90dup
ENST00000685664.1:c.1271-90dup ENSP00000509121.1:n.1271-90dup
ENST00000686381.1:c.1007-90dup ENSP00000509555.1:n.1007-90dup
ENST00000687065.1:c.1007-90dup ENSP00000510408.1:n.1007-90dup
ENST00000687394.1:n.1377-90dup
ENST00000687647.1:c.1007-90dup ENSP00000509205.1:n.1007-90dup
ENST00000688035.1:n.1686-90dup
ENST00000690315.1:c.1172-90dup ENSP00000509834.1:n.1172-90dup
ENST00000690373.1:n.1610-90dup
ENST00000690379.1:n.1301-90dup
ENST00000690824.1:c.1271-90dup ENSP00000510709.1:n.1271-90dup
ENST00000691661.1:c.1283-90dup ENSP00000510185.1:n.1283-90dup
ENST00000691862.1:c.1169-90dup ENSP00000509291.1:n.1169-90dup
ENST00000692813.1:c.1271-90dup ENSP00000509080.1:n.1271-90dup
ENST00000692972.1:c.1346-90dup ENSP00000510753.1:n.1346-90dup
ENST00000693454.1:n.481-90dup
ENST00000693602.1:n.1364-90dup
ENST00000358951.7:c.1271-90dup MANE Select ENSP00000351832.2:n.1271-90dup
ENST00000358951.6:c.1271-90dup ENSP00000351832.2:n.1271-90dup
ENST00000478976.1:n.292-949dup
NM_012414.3:c.1271-90dup NP_036546.2:n.1271-90dup
NM_012414.4:c.1271-90dup MANE Select NP_036546.2:n.1271-90dup