Canonical Allele Identifier: CA354047853
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413878C>T , CM000665.2:g.119413878C>T GRCh38
NC_000003.11:g.119132725C>T , CM000665.1:g.119132725C>T GRCh37
NC_000003.10:g.120615415C>T NCBI36
NG_007665.2:g.124506C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1949C>T MANE Select ENSP00000264245.4:p.Ala650Val
ENST00000264245.8:c.1949C>T ENSP00000264245.4:p.Ala650Val
NM_020754.3:c.1949C>T NP_065805.2:p.Ala650Val
XM_005247671.3:c.1856C>T XP_005247728.1:p.Ala619Val
XM_006713714.2:c.1889C>T XP_006713777.1:p.Ala630Val
XM_006713714.3:c.1889C>T XP_006713777.1:p.Ala630Val
XM_017006955.1:c.1457C>T XP_016862444.1:p.Ala486Val
NM_020754.4:c.1949C>T MANE Select NP_065805.2:p.Ala650Val