Canonical Allele Identifier: CA354051243
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414365A>C , CM000665.2:g.119414365A>C GRCh38
NC_000003.11:g.119133212A>C , CM000665.1:g.119133212A>C GRCh37
NC_000003.10:g.120615902A>C NCBI36
NG_007665.2:g.124993A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2436A>C MANE Select ENSP00000264245.4:p.Lys812Asn
ENST00000264245.8:c.2436A>C ENSP00000264245.4:p.Lys812Asn
NM_020754.3:c.2436A>C NP_065805.2:p.Lys812Asn
XM_005247671.3:c.2343A>C XP_005247728.1:p.Lys781Asn
XM_006713714.2:c.2376A>C XP_006713777.1:p.Lys792Asn
XM_006713714.3:c.2376A>C XP_006713777.1:p.Lys792Asn
XM_017006955.1:c.1944A>C XP_016862444.1:p.Lys648Asn
NM_020754.4:c.2436A>C MANE Select NP_065805.2:p.Lys812Asn