Canonical Allele Identifier: CA1396548320
Gene: ARHGAP31 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413494A= , CM000665.2:g.119413494A= GRCh38
NC_000003.11:g.119132341A= , CM000665.1:g.119132341A= GRCh37
NC_000003.10:g.120615031A= NCBI36
NG_007665.2:g.124122A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.1927-362A= MANE Select ENSP00000264245.4:n.1927-362A=
ENST00000264245.8:c.1927-362A= ENSP00000264245.4:n.1927-362A=
NM_020754.3:c.1927-362A= NP_065805.2:n.1927-362A=
XM_005247671.3:c.1834-362A= XP_005247728.1:n.1834-362A=
XM_006713714.2:c.1867-362A= XP_006713777.1:n.1867-362A=
XM_006713714.3:c.1867-362A= XP_006713777.1:n.1867-362A=
XM_017006955.1:c.1435-362A= XP_016862444.1:n.1435-362A=
NM_020754.4:c.1927-362A= MANE Select NP_065805.2:n.1927-362A=
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