Canonical Allele Identifier: CA12829534
Gene: XKR6 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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