Canonical Allele Identifier: CA1208109156
Gene: RABGAP1L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.174322729A= , CM000663.2:g.174322729A= GRCh38
NC_000001.10:g.174291867A= , CM000663.1:g.174291867A= GRCh37
NC_000001.9:g.172558490A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000681986.1:c.1465+17602A= MANE Select ENSP00000507884.1:n.1465+17602A=
ENST00000251507.8:c.1465+17602A= ENSP00000251507.4:n.1465+17602A=
ENST00000357444.10:c.1354+17602A= ENSP00000350027.6:n.1354+17602A=
ENST00000367690.5:c.406+17602A= ENSP00000489605.1:n.406+17602A=
ENST00000457696.1:c.1501+17602A= ENSP00000403136.1:n.1501+17602A=
NM_014857.4:c.1465+17602A= NP_055672.3:n.1465+17602A=
XM_005245680.1:c.1465+17602A= XP_005245737.1:n.1465+17602A=
XM_005245681.1:c.1354+17602A= XP_005245738.1:n.1354+17602A=
XM_006711693.1:c.1465+17602A= XP_006711756.1:n.1465+17602A=
XM_011510223.1:c.1465+17602A= XP_011508525.1:n.1465+17602A=
XR_922003.1:n.1672+17602A=
XR_922004.1:n.1672+17602A=
NM_001366445.1:c.1354+17602A= NP_001353374.1:n.1354+17602A=
NM_001366446.1:c.1465+17602A= MANE Select NP_001353375.1:n.1465+17602A=
NM_001366447.1:c.1354+17602A= NP_001353376.1:n.1354+17602A=
NM_001366448.1:c.1465+17602A= NP_001353377.1:n.1465+17602A=
NM_001366449.1:c.406+17602A= NP_001353378.1:n.406+17602A=
NR_158982.1:n.1636+17602A=
XM_005245681.2:c.1354+17602A= XP_005245738.1:n.1354+17602A=
XM_011510223.2:c.1465+17602A= XP_011508525.1:n.1465+17602A=
NM_014857.5:c.1465+17602A= NP_055672.3:n.1465+17602A=