Canonical Allele Identifier: CA354048505
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413967A>G , CM000665.2:g.119413967A>G GRCh38
NC_000003.11:g.119132814A>G , CM000665.1:g.119132814A>G GRCh37
NC_000003.10:g.120615504A>G NCBI36
NG_007665.2:g.124595A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2038A>G MANE Select ENSP00000264245.4:p.Ser680Gly
ENST00000264245.8:c.2038A>G ENSP00000264245.4:p.Ser680Gly
NM_020754.3:c.2038A>G NP_065805.2:p.Ser680Gly
XM_005247671.3:c.1945A>G XP_005247728.1:p.Ser649Gly
XM_006713714.2:c.1978A>G XP_006713777.1:p.Ser660Gly
XM_006713714.3:c.1978A>G XP_006713777.1:p.Ser660Gly
XM_017006955.1:c.1546A>G XP_016862444.1:p.Ser516Gly
NM_020754.4:c.2038A>G MANE Select NP_065805.2:p.Ser680Gly