Canonical Allele Identifier: CA412057881

Gene: ARHGAP6 AMELX

Linked Data

• MyVariant Identifiers: chrX:g.11316675C>G (hg19) ; chrX:g.11298555C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.11298555C>G , CM000685.2:g.11298555C>G	GRCh38
NC_000023.10:g.11316675C>G , CM000685.1:g.11316675C>G	GRCh37
NC_000023.9:g.11226596C>G	NCBI36
NG_012040.1:g.10143C>G
NG_012494.1:g.372147G>C
NG_012494.2:g.372147G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000337414.9:c.589-43848G>C (ARHGAP6) MANE Select	ENSP00000338967.4:n.589-43848G>C
ENST00000337414.8:c.589-43848G>C (ARHGAP6)	ENSP00000338967.4:n.589-43848G>C
ENST00000348912.4:c.104C>G (AMELX)	ENSP00000335312.5:p.Ser35Cys
ENST00000380712.7:c.194C>G (AMELX)	ENSP00000370088.3:p.Ser65Cys
ENST00000380714.7:c.152C>G (AMELX) MANE Select	ENSP00000370090.3:p.Ser51Cys
ENST00000380718.1:c.589-43848G>C (ARHGAP6)	ENSP00000370094.1:n.589-43848G>C
ENST00000380736.5:c.-21-43848G>C (ARHGAP6)	ENSP00000370112.1:n.-21-43848G>C
ENST00000489330.6:n.844-43848G>C (ARHGAP6)
ENST00000495242.5:c.589-8077G>C (ARHGAP6)	ENSP00000435767.1:n.589-8077G>C
NM_001142.2:c.152C>G (AMELX) MANE Select	NP_001133.1:p.Ser51Cys
NM_001287242.1:c.49-43848G>C (ARHGAP6)	NP_001274171.1:n.49-43848G>C
NM_006125.2:c.589-43848G>C (ARHGAP6)	NP_006116.2:n.589-43848G>C
NM_013427.2:c.589-43848G>C (ARHGAP6)	NP_038286.2:n.589-43848G>C
NM_182680.1:c.194C>G (AMELX)	NP_872621.1:p.Ser65Cys
NM_182681.1:c.104C>G (AMELX)	NP_872622.1:p.Ser35Cys
NR_109776.1:n.1462-8077G>C (ARHGAP6)
XM_011545489.1:c.194C>G (AMELX)	XP_011543791.1:p.Ser65Cys
XM_017029404.2:c.152C>G (AMELX)	XP_016884893.1:p.Ser51Cys
NM_013427.3:c.589-43848G>C (ARHGAP6) MANE Select	NP_038286.2:n.589-43848G>C
NM_001287242.2:c.49-43848G>C (ARHGAP6)	NP_001274171.1:n.49-43848G>C
NM_006125.3:c.589-43848G>C (ARHGAP6)	NP_006116.2:n.589-43848G>C
NR_109776.2:n.1681-8077G>C (ARHGAP6)