Canonical Allele Identifier: CA1473827676
Gene: ARHGAP24 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.85753128A= , CM000666.2:g.85753128A= GRCh38
NC_000004.11:g.86674281A= , CM000666.1:g.86674281A= GRCh37
NC_000004.10:g.86893305A= NCBI36
NG_051627.1:g.282998A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000395184.6:c.268+31156A= MANE Select ENSP00000378611.1:n.268+31156A=
ENST00000395184.5:c.268+31156A= ENSP00000378611.1:n.268+31156A=
ENST00000503995.5:c.268+31156A= ENSP00000423206.1:n.268+31156A=
ENST00000512201.5:c.-18+31156A= ENSP00000426105.1:n.-18+31156A=
NM_001025616.2:c.268+31156A= NP_001020787.2:n.268+31156A=
XM_005263263.3:c.268+31156A= XP_005263320.1:n.268+31156A=
XM_024454238.1:c.-18+31156A= XP_024310006.1:n.-18+31156A=
XM_024454239.1:c.-18+31156A= XP_024310007.1:n.-18+31156A=
NM_001025616.3:c.268+31156A= MANE Select NP_001020787.2:n.268+31156A=
Search 100 bp 5'
Search 100 bp 3'