Canonical Allele Identifier: CA1160545594
Gene: AHDC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.27550384_27550408delinsTGGCCGCTGCCACAGTGGCTGCCTC , CM000663.2:g.27550384_27550408delinsTGGCCGCTGCCACAGTGGCTGCCTC GRCh38
NC_000001.10:g.27876895_27876919delinsTGGCCGCTGCCACAGTGGCTGCCTC , CM000663.1:g.27876895_27876919delinsTGGCCGCTGCCACAGTGGCTGCCTC GRCh37
NC_000001.9:g.27749482_27749506delinsTGGCCGCTGCCACAGTGGCTGCCTC NCBI36
NG_034158.1:g.58087_58111delinsGAGGCAGCCACTGTGGCAGCGGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000247087.10:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA ENSP00000247087.4:p.Glu570=
ENST00000642245.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA ENSP00000495072.1:p.Glu570=
ENST00000642416.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA ENSP00000494394.1:p.Glu570=
ENST00000644989.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA ENSP00000495665.1:p.Glu570=
ENST00000673934.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA MANE Select ENSP00000501218.1:p.Glu570=
ENST00000247087.9:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA ENSP00000247087.4:p.Glu570=
ENST00000374011.6:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA ENSP00000363123.2:p.Glu570=
NM_001029882.3:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA NP_001025053.1:p.Glu570=
XM_005245848.2:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245905.1:p.Glu570=
XM_005245849.2:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245906.1:p.Glu570=
XM_005245850.2:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245907.1:p.Glu570=
XM_005245851.2:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245908.1:p.Glu570=
XM_005245852.2:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245909.1:p.Glu570=
XM_011541255.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_011539557.1:p.Glu570=
XM_011541256.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_011539558.1:p.Glu570=
XM_011541257.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_011539559.1:p.Glu570=
XR_946609.1:n.2665_2689delinsGAGGCAGCCACTGTGGCAGCGGCCA
XM_005245848.3:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245905.1:p.Glu570=
XM_005245849.3:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245906.1:p.Glu570=
XM_005245850.3:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245907.1:p.Glu570=
XM_005245851.3:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245908.1:p.Glu570=
XM_005245852.3:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_005245909.1:p.Glu570=
XM_011541256.2:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_011539558.1:p.Glu570=
XM_011541257.2:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_011539559.1:p.Glu570=
XM_024446461.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA XP_024302229.1:p.Glu570=
XR_946609.2:n.2775_2799delinsGAGGCAGCCACTGTGGCAGCGGCCA
NM_001371928.1:c.1708_1732delinsGAGGCAGCCACTGTGGCAGCGGCCA MANE Select NP_001358857.1:p.Glu570=