Canonical Allele Identifier: CA354049212
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1387076749

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414040G>C , CM000665.2:g.119414040G>C GRCh38
NC_000003.11:g.119132887G>C , CM000665.1:g.119132887G>C GRCh37
NC_000003.10:g.120615577G>C NCBI36
NG_007665.2:g.124668G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2111G>C MANE Select ENSP00000264245.4:p.Cys704Ser
ENST00000264245.8:c.2111G>C ENSP00000264245.4:p.Cys704Ser
NM_020754.3:c.2111G>C NP_065805.2:p.Cys704Ser
XM_005247671.3:c.2018G>C XP_005247728.1:p.Cys673Ser
XM_006713714.2:c.2051G>C XP_006713777.1:p.Cys684Ser
XM_006713714.3:c.2051G>C XP_006713777.1:p.Cys684Ser
XM_017006955.1:c.1619G>C XP_016862444.1:p.Cys540Ser
NM_020754.4:c.2111G>C MANE Select NP_065805.2:p.Cys704Ser