Canonical Allele Identifier: CA354047873
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413881T>C , CM000665.2:g.119413881T>C GRCh38
NC_000003.11:g.119132728T>C , CM000665.1:g.119132728T>C GRCh37
NC_000003.10:g.120615418T>C NCBI36
NG_007665.2:g.124509T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1952T>C MANE Select ENSP00000264245.4:p.Leu651Pro
ENST00000264245.8:c.1952T>C ENSP00000264245.4:p.Leu651Pro
NM_020754.3:c.1952T>C NP_065805.2:p.Leu651Pro
XM_005247671.3:c.1859T>C XP_005247728.1:p.Leu620Pro
XM_006713714.2:c.1892T>C XP_006713777.1:p.Leu631Pro
XM_006713714.3:c.1892T>C XP_006713777.1:p.Leu631Pro
XM_017006955.1:c.1460T>C XP_016862444.1:p.Leu487Pro
NM_020754.4:c.1952T>C MANE Select NP_065805.2:p.Leu651Pro