Canonical Allele Identifier: CA1129046565
Gene: NR6A1 HGNC NCBI

Linked Data

dbSNP Id: rs1834216624

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.124565616A>T , CM000671.2:g.124565616A>T GRCh38
NC_000009.11:g.127327895A>T , CM000671.1:g.127327895A>T GRCh37
NC_000009.10:g.126367716A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000487099.7:c.143-11046T>A MANE Select ENSP00000420267.1:n.143-11046T>A
ENST00000344523.8:c.143-11046T>A ENSP00000341135.4:n.143-11046T>A
ENST00000373584.7:c.143-11058T>A ENSP00000362686.3:n.143-11058T>A
ENST00000416460.6:c.143-11058T>A ENSP00000413701.2:n.143-11058T>A
ENST00000475178.1:c.17-11046T>A ENSP00000420587.1:n.17-11046T>A
ENST00000487099.6:c.143-11046T>A ENSP00000420267.1:n.143-11046T>A
NM_001278546.1:c.143-11058T>A NP_001265475.1:n.143-11058T>A
NM_001489.4:c.143-11058T>A NP_001480.3:n.143-11058T>A
NM_033334.3:c.143-11046T>A NP_201591.2:n.143-11046T>A
XM_005251917.3:c.143-11046T>A XP_005251974.1:n.143-11046T>A
XM_005251918.3:c.17-11046T>A XP_005251975.1:n.17-11046T>A
XM_005251917.5:c.143-11046T>A XP_005251974.1:n.143-11046T>A
XM_005251918.5:c.17-11046T>A XP_005251975.1:n.17-11046T>A
NM_033334.4:c.143-11046T>A MANE Select NP_201591.2:n.143-11046T>A
NM_001278546.2:c.143-11058T>A NP_001265475.1:n.143-11058T>A
NM_001489.5:c.143-11058T>A NP_001480.3:n.143-11058T>A