Canonical Allele Identifier: CA354050123
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119414189C>T , CM000665.2:g.119414189C>T GRCh38
NC_000003.11:g.119133036C>T , CM000665.1:g.119133036C>T GRCh37
NC_000003.10:g.120615726C>T NCBI36
NG_007665.2:g.124817C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000264245.9:c.2260C>T MANE Select ENSP00000264245.4:p.Pro754Ser
ENST00000264245.8:c.2260C>T ENSP00000264245.4:p.Pro754Ser
NM_020754.3:c.2260C>T NP_065805.2:p.Pro754Ser
XM_005247671.3:c.2167C>T XP_005247728.1:p.Pro723Ser
XM_006713714.2:c.2200C>T XP_006713777.1:p.Pro734Ser
XM_006713714.3:c.2200C>T XP_006713777.1:p.Pro734Ser
XM_017006955.1:c.1768C>T XP_016862444.1:p.Pro590Ser
NM_020754.4:c.2260C>T MANE Select NP_065805.2:p.Pro754Ser