Canonical Allele Identifier: CA2415488622

Gene: HCCS ARHGAP6

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11120866G= , CM000685.2:g.11120866G=	GRCh38
NC_000023.10:g.11138986G= , CM000685.1:g.11138986G=	GRCh37
NC_000023.9:g.11048907G=	NCBI36
NG_016460.1:g.14572G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000380762.5:c.522-41G= (HCCS) MANE Select	ENSP00000370139.4:n.522-41G=
ENST00000657361.1:c.1733-821C= (ARHGAP6)	ENSP00000499351.1:n.1733-821C=
ENST00000321143.8:c.522-41G= (HCCS)	ENSP00000326579.4:n.522-41G=
ENST00000380762.4:c.522-41G= (HCCS)	ENSP00000370139.4:n.522-41G=
ENST00000380763.7:c.522-41G= (HCCS)	ENSP00000370140.3:n.522-41G=
NM_001122608.2:c.522-41G= (HCCS)	NP_001116080.1:n.522-41G=
NM_001171991.2:c.522-41G= (HCCS)	NP_001165462.1:n.522-41G=
NM_005333.4:c.522-41G= (HCCS)	NP_005324.3:n.522-41G=
XM_024452368.1:c.582-41G= (HCCS)	XP_024308136.1:n.582-41G=
NM_005333.5:c.522-41G= (HCCS) MANE Select	NP_005324.3:n.522-41G=
NM_001122608.3:c.522-41G= (HCCS)	NP_001116080.1:n.522-41G=
NM_001171991.3:c.522-41G= (HCCS)	NP_001165462.1:n.522-41G=