Canonical Allele Identifier: CA354051360
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414382A>C , CM000665.2:g.119414382A>C GRCh38
NC_000003.11:g.119133229A>C , CM000665.1:g.119133229A>C GRCh37
NC_000003.10:g.120615919A>C NCBI36
NG_007665.2:g.125010A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2453A>C MANE Select ENSP00000264245.4:p.Tyr818Ser
ENST00000264245.8:c.2453A>C ENSP00000264245.4:p.Tyr818Ser
NM_020754.3:c.2453A>C NP_065805.2:p.Tyr818Ser
XM_005247671.3:c.2360A>C XP_005247728.1:p.Tyr787Ser
XM_006713714.2:c.2393A>C XP_006713777.1:p.Tyr798Ser
XM_006713714.3:c.2393A>C XP_006713777.1:p.Tyr798Ser
XM_017006955.1:c.1961A>C XP_016862444.1:p.Tyr654Ser
NM_020754.4:c.2453A>C MANE Select NP_065805.2:p.Tyr818Ser