Canonical Allele Identifier: CA1396542748

Gene: ARHGAP31

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.119399949T>C , CM000665.2:g.119399949T>C	GRCh38
NC_000003.11:g.119118796T>C , CM000665.1:g.119118796T>C	GRCh37
NC_000003.10:g.120601486T>C	NCBI36
NG_007665.2:g.110577T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264245.9:c.1069+688T>C MANE Select	ENSP00000264245.4:n.1069+688T>C
ENST00000264245.8:c.1069+688T>C	ENSP00000264245.4:n.1069+688T>C
NM_020754.3:c.1069+688T>C	NP_065805.2:n.1069+688T>C
XM_005247671.3:c.976+688T>C	XP_005247728.1:n.976+688T>C
XM_006713714.2:c.1069+688T>C	XP_006713777.1:n.1069+688T>C
XR_924388.1:n.202A>G
XM_006713714.3:c.1069+688T>C	XP_006713777.1:n.1069+688T>C
XM_017006955.1:c.577+688T>C	XP_016862444.1:n.577+688T>C
NM_020754.4:c.1069+688T>C MANE Select	NP_065805.2:n.1069+688T>C