Canonical Allele Identifier: CA891345642

Gene: RABGAP1L

Linked Data

• dbSNP Id: rs1254653463
• MyVariant Identifiers: chr1:g.174292006_174292007insTGCTG (hg19) ; chr1:g.174322868_174322869insTGCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.174322870_174322871insCTGTG , CM000663.2:g.174322870_174322871insCTGTG	GRCh38
NC_000001.10:g.174292008_174292009insCTGTG , CM000663.1:g.174292008_174292009insCTGTG	GRCh37
NC_000001.9:g.172558631_172558632insCTGTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000681986.1:c.1465+17743_1465+17744insCTGTG MANE Select	ENSP00000507884.1:n.1465+17743_1465+17744...
ENST00000251507.8:c.1465+17743_1465+17744insCTGTG	ENSP00000251507.4:n.1465+17743_1465+17744...
ENST00000357444.10:c.1354+17743_1354+17744insCTGTG	ENSP00000350027.6:n.1354+17743_1354+17744...
ENST00000367690.5:c.406+17743_406+17744insCTGTG	ENSP00000489605.1:n.406+17743_406+17744in...
ENST00000457696.1:c.1501+17743_1501+17744insCTGTG	ENSP00000403136.1:n.1501+17743_1501+17744...
NM_014857.4:c.1465+17743_1465+17744insCTGTG	NP_055672.3:n.1465+17743_1465+17744insCTG...
XM_005245680.1:c.1465+17743_1465+17744insCTGTG	XP_005245737.1:n.1465+17743_1465+17744ins...
XM_005245681.1:c.1354+17743_1354+17744insCTGTG	XP_005245738.1:n.1354+17743_1354+17744ins...
XM_006711693.1:c.1465+17743_1465+17744insCTGTG	XP_006711756.1:n.1465+17743_1465+17744ins...
XM_011510223.1:c.1465+17743_1465+17744insCTGTG	XP_011508525.1:n.1465+17743_1465+17744ins...
XR_922003.1:n.1672+17743_1672+17744insCTGTG
XR_922004.1:n.1672+17743_1672+17744insCTGTG
NM_001366445.1:c.1354+17743_1354+17744insCTGTG	NP_001353374.1:n.1354+17743_1354+17744ins...
NM_001366446.1:c.1465+17743_1465+17744insCTGTG MANE Select	NP_001353375.1:n.1465+17743_1465+17744ins...
NM_001366447.1:c.1354+17743_1354+17744insCTGTG	NP_001353376.1:n.1354+17743_1354+17744ins...
NM_001366448.1:c.1465+17743_1465+17744insCTGTG	NP_001353377.1:n.1465+17743_1465+17744ins...
NM_001366449.1:c.406+17743_406+17744insCTGTG	NP_001353378.1:n.406+17743_406+17744insCT...
NR_158982.1:n.1636+17743_1636+17744insCTGTG
XM_005245681.2:c.1354+17743_1354+17744insCTGTG	XP_005245738.1:n.1354+17743_1354+17744ins...
XM_011510223.2:c.1465+17743_1465+17744insCTGTG	XP_011508525.1:n.1465+17743_1465+17744ins...
NM_014857.5:c.1465+17743_1465+17744insCTGTG	NP_055672.3:n.1465+17743_1465+17744insCTG...