Canonical Allele Identifier: CA354047848
Gene: ARHGAP31 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.119413877G>T , CM000665.2:g.119413877G>T GRCh38
NC_000003.11:g.119132724G>T , CM000665.1:g.119132724G>T GRCh37
NC_000003.10:g.120615414G>T NCBI36
NG_007665.2:g.124505G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000264245.9:c.1948G>T MANE Select ENSP00000264245.4:p.Ala650Ser
ENST00000264245.8:c.1948G>T ENSP00000264245.4:p.Ala650Ser
NM_020754.3:c.1948G>T NP_065805.2:p.Ala650Ser
XM_005247671.3:c.1855G>T XP_005247728.1:p.Ala619Ser
XM_006713714.2:c.1888G>T XP_006713777.1:p.Ala630Ser
XM_006713714.3:c.1888G>T XP_006713777.1:p.Ala630Ser
XM_017006955.1:c.1456G>T XP_016862444.1:p.Ala486Ser
NM_020754.4:c.1948G>T MANE Select NP_065805.2:p.Ala650Ser