Canonical Allele Identifier: CA1763724598
Community Standard Title: NM_173683.4(XKR6):c.764+18269A=
Gene: XKR6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11182307T= , CM000670.2:g.11182307T= GRCh38
NC_000008.10:g.11039816T= , CM000670.1:g.11039816T= GRCh37
NC_000008.9:g.11077226T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_173683.4:c.764+18269A= MANE Select NP_775954.2:n.764+18269A=
ENST00000416569.3:c.764+18269A= MANE Select ENSP00000416707.2:n.764+18269A=
NM_173683.3:c.764+18269A= NP_775954.2:n.764+18269A=
NR_138152.1:n.922+12784A=
NR_138152.2:n.1389+12784A=
NR_138153.1:n.791+18269A=
NR_138153.2:n.1258+18269A=
NR_138154.1:n.791+18269A=
NR_138154.2:n.1258+18269A=
ENST00000416569.2:c.764+18269A= ENSP00000416707.2:n.764+18269A=
ENST00000529336.1:c.259+18269A=
XM_011543820.1:c.*31+12784A= XP_011542122.1:n.*31+12784A=
XM_024447129.1:c.764+18269A= XP_024302897.1:n.764+18269A=
XR_001745511.2:n.965+12784A=
XR_948899.1:n.937+12784A=
XR_948899.3:n.965+12784A=