Canonical Allele Identifier: CA343320237

Gene: ARHGAP30

Linked Data

• MyVariant Identifiers: chr1:g.161018073C>G (hg19) ; chr1:g.161048283C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161048283C>G , CM000663.2:g.161048283C>G	GRCh38
NC_000001.10:g.161018073C>G , CM000663.1:g.161018073C>G	GRCh37
NC_000001.9:g.159284697C>G	NCBI36
NG_011612.1:g.2685G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368013.8:c.2738G>C MANE Select	ENSP00000356992.3:p.Cys913Ser
ENST00000368013.7:c.2738G>C	ENSP00000356992.3:p.Cys913Ser
ENST00000368015.1:c.2207G>C	ENSP00000356994.1:p.Cys736Ser
ENST00000368016.7:c.2105G>C	ENSP00000356995.3:p.Cys702Ser
ENST00000461003.5:n.3520G>C
NM_001025598.1:c.2738G>C	NP_001020769.1:p.Cys913Ser
NM_001287600.1:c.2294G>C	NP_001274529.1:p.Cys765Ser
NM_001287602.1:c.2207G>C	NP_001274531.1:p.Cys736Ser
NM_181720.2:c.2105G>C	NP_859071.2:p.Cys702Ser
XM_005245070.2:c.2567G>C	XP_005245127.1:p.Cys856Ser
XM_005245071.3:c.2294G>C	XP_005245128.1:p.Cys765Ser
XM_005245073.2:c.2294G>C	XP_005245130.1:p.Cys765Ser
XM_011509391.1:c.2294G>C	XP_011507693.1:p.Cys765Ser
XM_005245073.3:c.2294G>C	XP_005245130.1:p.Cys765Ser
XM_011509391.2:c.2294G>C	XP_011507693.1:p.Cys765Ser
XM_017000960.1:c.2336G>C	XP_016856449.1:p.Cys779Ser
NM_001025598.2:c.2738G>C MANE Select	NP_001020769.1:p.Cys913Ser
NM_001287600.2:c.2294G>C	NP_001274529.1:p.Cys765Ser
NM_001287602.2:c.2207G>C	NP_001274531.1:p.Cys736Ser
NM_181720.3:c.2105G>C	NP_859071.2:p.Cys702Ser