Canonical Allele Identifier: CA515495874

Gene: HCCS ARHGAP6

Linked Data

• MyVariant Identifiers: chrX:g.11139027A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11120907A>C , CM000685.2:g.11120907A>C	GRCh38
NC_000023.10:g.11139027A>C , CM000685.1:g.11139027A>C	GRCh37
NC_000023.9:g.11048948A>C	NCBI36
NG_016460.1:g.14613A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000380762.5:c.522A>C (HCCS) MANE Select	ENSP00000370139.4:p.Ala174=
ENST00000657361.1:c.1733-862T>G (ARHGAP6)	ENSP00000499351.1:n.1733-862T>G
ENST00000321143.8:c.522A>C (HCCS)	ENSP00000326579.4:p.Ala174=
ENST00000380762.4:c.522A>C (HCCS)	ENSP00000370139.4:p.Ala174=
ENST00000380763.7:c.522A>C (HCCS)	ENSP00000370140.3:p.Ala174=
NM_001122608.2:c.522A>C (HCCS)	NP_001116080.1:p.Ala174=
NM_001171991.2:c.522A>C (HCCS)	NP_001165462.1:p.Ala174=
NM_005333.4:c.522A>C (HCCS)	NP_005324.3:p.Ala174=
XM_024452368.1:c.582A>C (HCCS)	XP_024308136.1:p.Ala194=
NM_005333.5:c.522A>C (HCCS) MANE Select	NP_005324.3:p.Ala174=
NM_001122608.3:c.522A>C (HCCS)	NP_001116080.1:p.Ala174=
NM_001171991.3:c.522A>C (HCCS)	NP_001165462.1:p.Ala174=