Canonical Allele Identifier: CA199908766

Gene: NR6A1

Linked Data

• dbSNP Id: rs113562364
• gnomAD v2: 9-127327737-TA-T
• gnomAD v3: 9-124565458-TA-T
• gnomAD v4: 9-124565458-TA-T
• MyVariant Identifiers: chr9:g.127327738del (hg19) ; chr9:g.124565459del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.124565467del , CM000671.2:g.124565467del	GRCh38
NC_000009.11:g.127327746del , CM000671.1:g.127327746del	GRCh37
NC_000009.10:g.126367567del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000487099.7:c.143-10889del MANE Select	ENSP00000420267.1:n.143-10889del
ENST00000344523.8:c.143-10889del	ENSP00000341135.4:n.143-10889del
ENST00000373584.7:c.143-10901del	ENSP00000362686.3:n.143-10901del
ENST00000416460.6:c.143-10901del	ENSP00000413701.2:n.143-10901del
ENST00000475178.1:c.17-10889del	ENSP00000420587.1:n.17-10889del
ENST00000487099.6:c.143-10889del	ENSP00000420267.1:n.143-10889del
NM_001278546.1:c.143-10901del	NP_001265475.1:n.143-10901del
NM_001489.4:c.143-10901del	NP_001480.3:n.143-10901del
NM_033334.3:c.143-10889del	NP_201591.2:n.143-10889del
XM_005251917.3:c.143-10889del	XP_005251974.1:n.143-10889del
XM_005251918.3:c.17-10889del	XP_005251975.1:n.17-10889del
XM_005251917.5:c.143-10889del	XP_005251974.1:n.143-10889del
XM_005251918.5:c.17-10889del	XP_005251975.1:n.17-10889del
NM_033334.4:c.143-10889del MANE Select	NP_201591.2:n.143-10889del
NM_001278546.2:c.143-10901del	NP_001265475.1:n.143-10901del
NM_001489.5:c.143-10901del	NP_001480.3:n.143-10901del