Canonical Allele Identifier: CA354051296
Gene: ARHGAP31 HGNC NCBI

Linked Data

dbSNP Id: rs1432145600

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414371G>T , CM000665.2:g.119414371G>T GRCh38
NC_000003.11:g.119133218G>T , CM000665.1:g.119133218G>T GRCh37
NC_000003.10:g.120615908G>T NCBI36
NG_007665.2:g.124999G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2442G>T MANE Select ENSP00000264245.4:p.Arg814Ser
ENST00000264245.8:c.2442G>T ENSP00000264245.4:p.Arg814Ser
NM_020754.3:c.2442G>T NP_065805.2:p.Arg814Ser
XM_005247671.3:c.2349G>T XP_005247728.1:p.Arg783Ser
XM_006713714.2:c.2382G>T XP_006713777.1:p.Arg794Ser
XM_006713714.3:c.2382G>T XP_006713777.1:p.Arg794Ser
XM_017006955.1:c.1950G>T XP_016862444.1:p.Arg650Ser
NM_020754.4:c.2442G>T MANE Select NP_065805.2:p.Arg814Ser