Canonical Allele Identifier: CA1396521108

Gene: ARHGAP31

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119349465A>G , CM000665.2:g.119349465A>G	GRCh38
NC_000003.11:g.119068312A>G , CM000665.1:g.119068312A>G	GRCh37
NC_000003.10:g.120551002A>G	NCBI36
NG_007665.2:g.60093A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.101-15851A>G MANE Select	ENSP00000264245.4:n.101-15851A>G
ENST00000264245.8:c.101-15851A>G	ENSP00000264245.4:n.101-15851A>G
ENST00000482743.1:c.14-15851A>G	ENSP00000418429.1:n.14-15851A>G
NM_020754.3:c.101-15851A>G	NP_065805.2:n.101-15851A>G
XM_005247671.3:c.8-15851A>G	XP_005247728.1:n.8-15851A>G
XM_006713714.2:c.101-15851A>G	XP_006713777.1:n.101-15851A>G
XM_006713714.3:c.101-15851A>G	XP_006713777.1:n.101-15851A>G
XM_017006955.1:c.-247-15851A>G	XP_016862444.1:n.-247-15851A>G
NM_020754.4:c.101-15851A>G MANE Select	NP_065805.2:n.101-15851A>G