Canonical Allele Identifier: CA344645770

Gene: RAB3GAP2

Linked Data

• MyVariant Identifiers: chr1:g.220364623T>G (hg19) ; chr1:g.220191281T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.220191281T>G , CM000663.2:g.220191281T>G	GRCh38
NC_000001.10:g.220364623T>G , CM000663.1:g.220364623T>G	GRCh37
NC_000001.9:g.218431246T>G	NCBI36
NG_015837.1:g.86221A>C
NG_015837.2:g.86221A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685286.1:c.1274A>C	ENSP00000509457.1:p.Tyr425Ser
ENST00000685664.1:c.1274A>C	ENSP00000509121.1:p.Tyr425Ser
ENST00000686381.1:c.1010A>C	ENSP00000509555.1:p.Tyr337Ser
ENST00000687065.1:c.1010A>C	ENSP00000510408.1:p.Tyr337Ser
ENST00000687394.1:n.1380A>C
ENST00000687647.1:c.1010A>C	ENSP00000509205.1:p.Tyr337Ser
ENST00000688035.1:n.1689A>C
ENST00000690315.1:c.1175A>C	ENSP00000509834.1:p.Tyr392Ser
ENST00000690373.1:n.1613A>C
ENST00000690379.1:n.1304A>C
ENST00000690824.1:c.1274A>C	ENSP00000510709.1:p.Tyr425Ser
ENST00000691661.1:c.1286A>C	ENSP00000510185.1:p.Tyr429Ser
ENST00000691862.1:c.1172A>C	ENSP00000509291.1:p.Tyr391Ser
ENST00000692813.1:c.1274A>C	ENSP00000509080.1:p.Tyr425Ser
ENST00000692972.1:c.1349A>C	ENSP00000510753.1:p.Tyr450Ser
ENST00000693454.1:n.484A>C
ENST00000693602.1:n.1367A>C
ENST00000358951.7:c.1274A>C MANE Select	ENSP00000351832.2:p.Tyr425Ser
ENST00000358951.6:c.1274A>C	ENSP00000351832.2:p.Tyr425Ser
ENST00000478976.1:n.292-856A>C
NM_012414.3:c.1274A>C	NP_036546.2:p.Tyr425Ser
NM_012414.4:c.1274A>C MANE Select	NP_036546.2:p.Tyr425Ser