Canonical Allele Identifier: CA288066987
Gene: ARHGAP44 HGNC NCBI
COSMIC:
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.12874085A>G , CM000679.2:g.12874085A>G GRCh38
NC_000017.10:g.12777402A>G , CM000679.1:g.12777402A>G GRCh37
NC_000017.9:g.12718127A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000379672.10:c.54-20855A>G MANE Select ENSP00000368994.5:n.54-20855A>G
ENST00000262444.13:c.54-20855A>G ENSP00000262444.9:n.54-20855A>G
ENST00000340825.7:c.54-20855A>G ENSP00000342566.3:n.54-20855A>G
ENST00000379672.9:c.54-20855A>G ENSP00000368994.5:n.54-20855A>G
ENST00000544416.6:c.54-20855A>G ENSP00000437542.2:n.54-20855A>G
ENST00000578442.1:n.256-20855A>G
ENST00000580768.5:c.54-20855A>G ENSP00000462141.1:n.54-20855A>G
NM_014859.4:c.54-20855A>G NP_055674.4:n.54-20855A>G
XM_005256888.1:c.54-20855A>G XP_005256945.1:n.54-20855A>G
XM_005256889.2:c.54-20855A>G XP_005256946.1:n.54-20855A>G
XM_005256890.1:c.54-20855A>G XP_005256947.1:n.54-20855A>G
XM_005256891.1:c.54-20855A>G XP_005256948.1:n.54-20855A>G
XM_006721615.1:c.54-20855A>G XP_006721678.1:n.54-20855A>G
NM_001321164.1:c.54-20855A>G NP_001308093.1:n.54-20855A>G
NM_001321166.1:c.54-20855A>G NP_001308095.1:n.54-20855A>G
NM_001321167.1:c.54-20855A>G NP_001308096.1:n.54-20855A>G
NM_001321168.1:c.-429-20855A>G NP_001308097.1:n.-429-20855A>G
NM_014859.5:c.54-20855A>G NP_055674.4:n.54-20855A>G
NR_135569.1:n.381-20855A>G
XM_005256891.2:c.54-20855A>G XP_005256948.1:n.54-20855A>G
NM_014859.6:c.54-20855A>G MANE Select NP_055674.4:n.54-20855A>G
NM_001321164.2:c.54-20855A>G NP_001308093.1:n.54-20855A>G
NM_001321166.2:c.54-20855A>G NP_001308095.1:n.54-20855A>G
NM_001321167.2:c.54-20855A>G NP_001308096.1:n.54-20855A>G
NM_001321168.2:c.-429-20855A>G NP_001308097.1:n.-429-20855A>G
NR_135569.2:n.395-20855A>G