Canonical Allele Identifier: CA1203938

Gene: ARHGAP30

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161047766C>T , CM000663.2:g.161047766C>T	GRCh38
NC_000001.10:g.161017556C>T , CM000663.1:g.161017556C>T	GRCh37
NC_000001.9:g.159284180C>T	NCBI36
NG_011612.1:g.3202G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368013.8:c.3255G>A MANE Select	ENSP00000356992.3:p.Arg1085=
ENST00000368013.7:c.3255G>A	ENSP00000356992.3:p.Arg1085=
ENST00000368015.1:c.2724G>A	ENSP00000356994.1:p.Arg908=
ENST00000368016.7:c.2622G>A	ENSP00000356995.3:p.Arg874=
ENST00000461003.5:n.4037G>A
NM_001025598.1:c.3255G>A	NP_001020769.1:p.Arg1085=
NM_001287600.1:c.2811G>A	NP_001274529.1:p.Arg937=
NM_001287602.1:c.2724G>A	NP_001274531.1:p.Arg908=
NM_181720.2:c.2622G>A	NP_859071.2:p.Arg874=
XM_005245070.2:c.3084G>A	XP_005245127.1:p.Arg1028=
XM_005245071.3:c.2811G>A	XP_005245128.1:p.Arg937=
XM_005245073.2:c.2811G>A	XP_005245130.1:p.Arg937=
XM_011509391.1:c.2811G>A	XP_011507693.1:p.Arg937=
XM_005245073.3:c.2811G>A	XP_005245130.1:p.Arg937=
XM_011509391.2:c.2811G>A	XP_011507693.1:p.Arg937=
XM_017000960.1:c.2853G>A	XP_016856449.1:p.Arg951=
NM_001025598.2:c.3255G>A MANE Select	NP_001020769.1:p.Arg1085=
NM_001287600.2:c.2811G>A	NP_001274529.1:p.Arg937=
NM_001287602.2:c.2724G>A	NP_001274531.1:p.Arg908=
NM_181720.3:c.2622G>A	NP_859071.2:p.Arg874=