Canonical Allele Identifier: CA845658493

Gene: XKR6

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11187652G>T , CM000670.2:g.11187652G>T	GRCh38
NC_000008.10:g.11045161G>T , CM000670.1:g.11045161G>T	GRCh37
NC_000008.9:g.11082571G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000416569.3:c.764+12924C>A MANE Select	ENSP00000416707.2:n.764+12924C>A
ENST00000416569.2:c.764+12924C>A	ENSP00000416707.2:n.764+12924C>A
ENST00000529336.1:c.259+12924C>A
NM_173683.3:c.764+12924C>A	NP_775954.2:n.764+12924C>A
XM_011543820.1:c.*31+7439C>A	XP_011542122.1:n.*31+7439C>A
XR_948899.1:n.937+7439C>A
NR_138152.1:n.922+7439C>A
NR_138153.1:n.791+12924C>A
NR_138154.1:n.791+12924C>A
XM_024447129.1:c.764+12924C>A	XP_024302897.1:n.764+12924C>A
XR_001745511.2:n.965+7439C>A
XR_948899.3:n.965+7439C>A
NM_173683.4:c.764+12924C>A MANE Select	NP_775954.2:n.764+12924C>A
NR_138152.2:n.1389+7439C>A
NR_138153.2:n.1258+12924C>A
NR_138154.2:n.1258+12924C>A