Canonical Allele Identifier: CA671578840

Gene: ARHGAP20

Linked Data

• dbSNP Id: rs1336079369
• MyVariant Identifiers: chr11:g.110499161T>A (hg19) ; chr11:g.110628438T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.110628438T>A , CM000673.2:g.110628438T>A	GRCh38
NC_000011.9:g.110499161T>A , CM000673.1:g.110499161T>A	GRCh37
NC_000011.8:g.110004371T>A	NCBI36
NG_051657.1:g.89752A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683387.1:c.353+2190A>T MANE Select	ENSP00000507405.1:n.353+2190A>T
ENST00000260283.8:c.353+2190A>T	ENSP00000260283.4:n.353+2190A>T
ENST00000524756.5:c.284+2190A>T	ENSP00000432076.1:n.284+2190A>T
ENST00000527598.1:c.245+2190A>T	ENSP00000431399.1:n.245+2190A>T
ENST00000528829.5:c.245+2190A>T	ENSP00000436319.1:n.245+2190A>T
ENST00000533353.5:c.275+2190A>T	ENSP00000436522.1:n.275+2190A>T
NM_001258415.1:c.284+2190A>T	NP_001245344.1:n.284+2190A>T
NM_001258416.1:c.275+2190A>T	NP_001245345.1:n.275+2190A>T
NM_001258417.1:c.245+2190A>T	NP_001245346.1:n.245+2190A>T
NM_001258418.1:c.245+2190A>T	NP_001245347.1:n.245+2190A>T
NM_020809.3:c.353+2190A>T	NP_065860.2:n.353+2190A>T
XM_006718893.2:c.353+2190A>T	XP_006718956.1:n.353+2190A>T
XM_006718893.3:c.353+2190A>T	XP_006718956.1:n.353+2190A>T
NM_001258415.2:c.284+2190A>T	NP_001245344.1:n.284+2190A>T
NM_001258416.2:c.275+2190A>T	NP_001245345.1:n.275+2190A>T
NM_001258417.2:c.245+2190A>T	NP_001245346.1:n.245+2190A>T
NM_001258418.2:c.245+2190A>T	NP_001245347.1:n.245+2190A>T
NM_001384657.1:c.353+2190A>T MANE Select	NP_001371586.1:n.353+2190A>T
NM_020809.4:c.353+2190A>T	NP_065860.2:n.353+2190A>T