Canonical Allele Identifier: CA412055177

Gene: HCCS ARHGAP6

Linked Data

• MyVariant Identifiers: chrX:g.11139039T>A (hg19) ; chrX:g.11120919T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11120919T>A , CM000685.2:g.11120919T>A	GRCh38
NC_000023.10:g.11139039T>A , CM000685.1:g.11139039T>A	GRCh37
NC_000023.9:g.11048960T>A	NCBI36
NG_016460.1:g.14625T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380762.5:c.534T>A (HCCS) MANE Select	ENSP00000370139.4:p.Cys178Ter
ENST00000657361.1:c.1733-874A>T (ARHGAP6)	ENSP00000499351.1:n.1733-874A>T
ENST00000321143.8:c.534T>A (HCCS)	ENSP00000326579.4:p.Cys178Ter
ENST00000380762.4:c.534T>A (HCCS)	ENSP00000370139.4:p.Cys178Ter
ENST00000380763.7:c.534T>A (HCCS)	ENSP00000370140.3:p.Cys178Ter
NM_001122608.2:c.534T>A (HCCS)	NP_001116080.1:p.Cys178Ter
NM_001171991.2:c.534T>A (HCCS)	NP_001165462.1:p.Cys178Ter
NM_005333.4:c.534T>A (HCCS)	NP_005324.3:p.Cys178Ter
XM_024452368.1:c.594T>A (HCCS)	XP_024308136.1:p.Cys198Ter
NM_005333.5:c.534T>A (HCCS) MANE Select	NP_005324.3:p.Cys178Ter
NM_001122608.3:c.534T>A (HCCS)	NP_001116080.1:p.Cys178Ter
NM_001171991.3:c.534T>A (HCCS)	NP_001165462.1:p.Cys178Ter