Canonical Allele Identifier: CA414759924

Gene: ARHGEF6

Linked Data

• MyVariant Identifiers: chrX:g.135761754A>C (hg19) ; chrX:g.136679595A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.136679595A>C , CM000685.2:g.136679595A>C	GRCh38
NC_000023.10:g.135761754A>C , CM000685.1:g.135761754A>C	GRCh37
NC_000023.9:g.135589420A>C	NCBI36
NG_008873.1:g.106750T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000250617.7:c.1770T>G MANE Select	ENSP00000250617.6:p.Ser590Arg
ENST00000250617.6:c.1770T>G	ENSP00000250617.6:p.Ser590Arg
ENST00000370620.5:c.1308T>G	ENSP00000359654.1:p.Ser436Arg
ENST00000370622.5:c.1308T>G	ENSP00000359656.1:p.Ser436Arg
NM_001306177.1:c.1308T>G	NP_001293106.1:p.Ser436Arg
NM_004840.2:c.1770T>G	NP_004831.1:p.Ser590Arg
XM_005262499.2:c.1704+1136T>G	XP_005262556.1:n.1704+1136T>G
XM_011531412.1:c.1851T>G	XP_011529714.1:p.Ser617Arg
XM_011531413.1:c.1782T>G	XP_011529715.1:p.Ser594Arg
XM_011531414.1:c.1782T>G	XP_011529716.1:p.Ser594Arg
XM_011531415.1:c.1680T>G	XP_011529717.1:p.Ser560Arg
XM_011531416.1:c.1389T>G	XP_011529718.1:p.Ser463Arg
XM_011531417.1:c.1320T>G	XP_011529719.1:p.Ser440Arg
XM_005262499.3:c.1704+1136T>G	XP_005262556.1:n.1704+1136T>G
XM_011531412.3:c.1851T>G	XP_011529714.1:p.Ser617Arg
XM_011531413.2:c.1782T>G	XP_011529715.1:p.Ser594Arg
XM_011531414.2:c.1782T>G	XP_011529716.1:p.Ser594Arg
XM_011531415.3:c.1680T>G	XP_011529717.1:p.Ser560Arg
XM_011531416.3:c.1389T>G	XP_011529718.1:p.Ser463Arg
XM_017029975.2:c.1863T>G	XP_016885464.1:p.Ser621Arg
NM_004840.3:c.1770T>G MANE Select	NP_004831.1:p.Ser590Arg
NM_001306177.2:c.1308T>G	NP_001293106.1:p.Ser436Arg