Canonical Allele Identifier: CA1999907684

Gene: ARHGAP20

Linked Data

• dbSNP Id: rs1948792218

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110628480A>G , CM000673.2:g.110628480A>G	GRCh38
NC_000011.9:g.110499203A>G , CM000673.1:g.110499203A>G	GRCh37
NC_000011.8:g.110004413A>G	NCBI36
NG_051657.1:g.89710T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683387.1:c.353+2148T>C MANE Select	ENSP00000507405.1:n.353+2148T>C
ENST00000260283.8:c.353+2148T>C	ENSP00000260283.4:n.353+2148T>C
ENST00000524756.5:c.284+2148T>C	ENSP00000432076.1:n.284+2148T>C
ENST00000527598.1:c.245+2148T>C	ENSP00000431399.1:n.245+2148T>C
ENST00000528829.5:c.245+2148T>C	ENSP00000436319.1:n.245+2148T>C
ENST00000533353.5:c.275+2148T>C	ENSP00000436522.1:n.275+2148T>C
NM_001258415.1:c.284+2148T>C	NP_001245344.1:n.284+2148T>C
NM_001258416.1:c.275+2148T>C	NP_001245345.1:n.275+2148T>C
NM_001258417.1:c.245+2148T>C	NP_001245346.1:n.245+2148T>C
NM_001258418.1:c.245+2148T>C	NP_001245347.1:n.245+2148T>C
NM_020809.3:c.353+2148T>C	NP_065860.2:n.353+2148T>C
XM_006718893.2:c.353+2148T>C	XP_006718956.1:n.353+2148T>C
XM_006718893.3:c.353+2148T>C	XP_006718956.1:n.353+2148T>C
NM_001258415.2:c.284+2148T>C	NP_001245344.1:n.284+2148T>C
NM_001258416.2:c.275+2148T>C	NP_001245345.1:n.275+2148T>C
NM_001258417.2:c.245+2148T>C	NP_001245346.1:n.245+2148T>C
NM_001258418.2:c.245+2148T>C	NP_001245347.1:n.245+2148T>C
NM_001384657.1:c.353+2148T>C MANE Select	NP_001371586.1:n.353+2148T>C
NM_020809.4:c.353+2148T>C	NP_065860.2:n.353+2148T>C