Canonical Allele Identifier: CA354050764
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414285C>G , CM000665.2:g.119414285C>G GRCh38
NC_000003.11:g.119133132C>G , CM000665.1:g.119133132C>G GRCh37
NC_000003.10:g.120615822C>G NCBI36
NG_007665.2:g.124913C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2356C>G MANE Select ENSP00000264245.4:p.Pro786Ala
ENST00000264245.8:c.2356C>G ENSP00000264245.4:p.Pro786Ala
NM_020754.3:c.2356C>G NP_065805.2:p.Pro786Ala
XM_005247671.3:c.2263C>G XP_005247728.1:p.Pro755Ala
XM_006713714.2:c.2296C>G XP_006713777.1:p.Pro766Ala
XM_006713714.3:c.2296C>G XP_006713777.1:p.Pro766Ala
XM_017006955.1:c.1864C>G XP_016862444.1:p.Pro622Ala
NM_020754.4:c.2356C>G MANE Select NP_065805.2:p.Pro786Ala