Canonical Allele Identifier: CA1160545609

Gene: AHDC1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.27550413_27550416delinsGCCA , CM000663.2:g.27550413_27550416delinsGCCA	GRCh38
NC_000001.10:g.27876924_27876927delinsGCCA , CM000663.1:g.27876924_27876927delinsGCCA	GRCh37
NC_000001.9:g.27749511_27749514delinsGCCA	NCBI36
NG_034158.1:g.58079_58082delinsTGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000247087.10:c.1700_1703delinsTGGC	ENSP00000247087.4:p.Val567=
ENST00000642245.1:c.1700_1703delinsTGGC	ENSP00000495072.1:p.Val567=
ENST00000642416.1:c.1700_1703delinsTGGC	ENSP00000494394.1:p.Val567=
ENST00000644989.1:c.1700_1703delinsTGGC	ENSP00000495665.1:p.Val567=
ENST00000673934.1:c.1700_1703delinsTGGC MANE Select	ENSP00000501218.1:p.Val567=
ENST00000247087.9:c.1700_1703delinsTGGC	ENSP00000247087.4:p.Val567=
ENST00000374011.6:c.1700_1703delinsTGGC	ENSP00000363123.2:p.Val567=
NM_001029882.3:c.1700_1703delinsTGGC	NP_001025053.1:p.Val567=
XM_005245848.2:c.1700_1703delinsTGGC	XP_005245905.1:p.Val567=
XM_005245849.2:c.1700_1703delinsTGGC	XP_005245906.1:p.Val567=
XM_005245850.2:c.1700_1703delinsTGGC	XP_005245907.1:p.Val567=
XM_005245851.2:c.1700_1703delinsTGGC	XP_005245908.1:p.Val567=
XM_005245852.2:c.1700_1703delinsTGGC	XP_005245909.1:p.Val567=
XM_011541255.1:c.1700_1703delinsTGGC	XP_011539557.1:p.Val567=
XM_011541256.1:c.1700_1703delinsTGGC	XP_011539558.1:p.Val567=
XM_011541257.1:c.1700_1703delinsTGGC	XP_011539559.1:p.Val567=
XR_946609.1:n.2657_2660delinsTGGC
XM_005245848.3:c.1700_1703delinsTGGC	XP_005245905.1:p.Val567=
XM_005245849.3:c.1700_1703delinsTGGC	XP_005245906.1:p.Val567=
XM_005245850.3:c.1700_1703delinsTGGC	XP_005245907.1:p.Val567=
XM_005245851.3:c.1700_1703delinsTGGC	XP_005245908.1:p.Val567=
XM_005245852.3:c.1700_1703delinsTGGC	XP_005245909.1:p.Val567=
XM_011541256.2:c.1700_1703delinsTGGC	XP_011539558.1:p.Val567=
XM_011541257.2:c.1700_1703delinsTGGC	XP_011539559.1:p.Val567=
XM_024446461.1:c.1700_1703delinsTGGC	XP_024302229.1:p.Val567=
XR_946609.2:n.2767_2770delinsTGGC
NM_001371928.1:c.1700_1703delinsTGGC MANE Select	NP_001358857.1:p.Val567=