Canonical Allele Identifier: CA15088160
Gene: RABGAP1L HGNC NCBI

Linked Data

dbSNP Id: rs10912765

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.174322812C>G , CM000663.2:g.174322812C>G GRCh38
NC_000001.10:g.174291950C>G , CM000663.1:g.174291950C>G GRCh37
NC_000001.9:g.172558573C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000681986.1:c.1465+17685C>G MANE Select ENSP00000507884.1:n.1465+17685C>G
ENST00000251507.8:c.1465+17685C>G ENSP00000251507.4:n.1465+17685C>G
ENST00000357444.10:c.1354+17685C>G ENSP00000350027.6:n.1354+17685C>G
ENST00000367690.5:c.406+17685C>G ENSP00000489605.1:n.406+17685C>G
ENST00000457696.1:c.1501+17685C>G ENSP00000403136.1:n.1501+17685C>G
NM_014857.4:c.1465+17685C>G NP_055672.3:n.1465+17685C>G
XM_005245680.1:c.1465+17685C>G XP_005245737.1:n.1465+17685C>G
XM_005245681.1:c.1354+17685C>G XP_005245738.1:n.1354+17685C>G
XM_006711693.1:c.1465+17685C>G XP_006711756.1:n.1465+17685C>G
XM_011510223.1:c.1465+17685C>G XP_011508525.1:n.1465+17685C>G
XR_922003.1:n.1672+17685C>G
XR_922004.1:n.1672+17685C>G
NM_001366445.1:c.1354+17685C>G NP_001353374.1:n.1354+17685C>G
NM_001366446.1:c.1465+17685C>G MANE Select NP_001353375.1:n.1465+17685C>G
NM_001366447.1:c.1354+17685C>G NP_001353376.1:n.1354+17685C>G
NM_001366448.1:c.1465+17685C>G NP_001353377.1:n.1465+17685C>G
NM_001366449.1:c.406+17685C>G NP_001353378.1:n.406+17685C>G
NR_158982.1:n.1636+17685C>G
XM_005245681.2:c.1354+17685C>G XP_005245738.1:n.1354+17685C>G
XM_011510223.2:c.1465+17685C>G XP_011508525.1:n.1465+17685C>G
NM_014857.5:c.1465+17685C>G NP_055672.3:n.1465+17685C>G