Canonical Allele Identifier: CA344645650

Gene: RAB3GAP2

Linked Data

• MyVariant Identifiers: chr1:g.220364571T>A (hg19) ; chr1:g.220191229T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220191229T>A , CM000663.2:g.220191229T>A	GRCh38
NC_000001.10:g.220364571T>A , CM000663.1:g.220364571T>A	GRCh37
NC_000001.9:g.218431194T>A	NCBI36
NG_015837.1:g.86273A>T
NG_015837.2:g.86273A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685286.1:c.1326A>T	ENSP00000509457.1:p.Arg442Ser
ENST00000685664.1:c.1326A>T	ENSP00000509121.1:p.Arg442Ser
ENST00000686381.1:c.1062A>T	ENSP00000509555.1:p.Arg354Ser
ENST00000687065.1:c.1062A>T	ENSP00000510408.1:p.Arg354Ser
ENST00000687394.1:n.1432A>T
ENST00000687647.1:c.1062A>T	ENSP00000509205.1:p.Arg354Ser
ENST00000688035.1:n.1741A>T
ENST00000690315.1:c.1227A>T	ENSP00000509834.1:p.Arg409Ser
ENST00000690373.1:n.1665A>T
ENST00000690379.1:n.1356A>T
ENST00000690824.1:c.1326A>T	ENSP00000510709.1:p.Arg442Ser
ENST00000691661.1:c.1338A>T	ENSP00000510185.1:p.Arg446Ser
ENST00000691862.1:c.1224A>T	ENSP00000509291.1:p.Arg408Ser
ENST00000692813.1:c.1326A>T	ENSP00000509080.1:p.Arg442Ser
ENST00000692972.1:c.1401A>T	ENSP00000510753.1:p.Arg467Ser
ENST00000693454.1:n.536A>T
ENST00000693602.1:n.1419A>T
ENST00000358951.7:c.1326A>T MANE Select	ENSP00000351832.2:p.Arg442Ser
ENST00000358951.6:c.1326A>T	ENSP00000351832.2:p.Arg442Ser
ENST00000478976.1:n.292-804A>T
NM_012414.3:c.1326A>T	NP_036546.2:p.Arg442Ser
NM_012414.4:c.1326A>T MANE Select	NP_036546.2:p.Arg442Ser