Canonical Allele Identifier: CA10692252
Gene: RABGAP1L HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17301853

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.174583673C>T , CM000663.2:g.174583673C>T GRCh38
NC_000001.10:g.174552811C>T , CM000663.1:g.174552811C>T GRCh37
NC_000001.9:g.172819434C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_014857.4:c.1711-53702C>T VV NP_055672.3:p.=
XM_005245680.1:c.1711-53702C>T XP_005245737.1:p.=
XM_005245681.1:c.1600-53702C>T XP_005245738.1:p.=
XM_006711693.1:c.1711-53702C>T XP_006711756.1:p.=
XM_011510223.1:c.1711-53702C>T XP_011508525.1:p.=
XR_922003.1:n.1918-53702C>T
XR_922004.1:n.1918-53702C>T
NM_001366446.1:c.1711-53702C>T VV NP_001353375.1:p.=
NM_001366447.1:c.1600-53702C>T VV NP_001353376.1:p.=
NM_001366448.1:c.1711-53702C>T VV NP_001353377.1:p.=
NR_158982.1:n.1882-53702C>T
XM_005245681.2:c.1600-53702C>T XP_005245738.1:p.=
XM_011510223.2:c.1711-53702C>T XP_011508525.1:p.=
ENST00000251507.8:c.1711-53702C>T ENSP00000251507.4:p.=
ENST00000526253.1:n.326-53702C>T