Canonical Allele Identifier: CA343317996

Gene: ARHGAP30

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368013.8:c.3255G>T MANE Select	ENSP00000356992.3:p.Arg1085Ser
ENST00000368013.7:c.3255G>T	ENSP00000356992.3:p.Arg1085Ser
ENST00000368015.1:c.2724G>T	ENSP00000356994.1:p.Arg908Ser
ENST00000368016.7:c.2622G>T	ENSP00000356995.3:p.Arg874Ser
ENST00000461003.5:n.4037G>T
NM_001025598.1:c.3255G>T	NP_001020769.1:p.Arg1085Ser
NM_001287600.1:c.2811G>T	NP_001274529.1:p.Arg937Ser
NM_001287602.1:c.2724G>T	NP_001274531.1:p.Arg908Ser
NM_181720.2:c.2622G>T	NP_859071.2:p.Arg874Ser
XM_005245070.2:c.3084G>T	XP_005245127.1:p.Arg1028Ser
XM_005245071.3:c.2811G>T	XP_005245128.1:p.Arg937Ser
XM_005245073.2:c.2811G>T	XP_005245130.1:p.Arg937Ser
XM_011509391.1:c.2811G>T	XP_011507693.1:p.Arg937Ser
XM_005245073.3:c.2811G>T	XP_005245130.1:p.Arg937Ser
XM_011509391.2:c.2811G>T	XP_011507693.1:p.Arg937Ser
XM_017000960.1:c.2853G>T	XP_016856449.1:p.Arg951Ser
NM_001025598.2:c.3255G>T MANE Select	NP_001020769.1:p.Arg1085Ser
NM_001287600.2:c.2811G>T	NP_001274529.1:p.Arg937Ser
NM_001287602.2:c.2724G>T	NP_001274531.1:p.Arg908Ser
NM_181720.3:c.2622G>T	NP_859071.2:p.Arg874Ser