Canonical Allele Identifier: CA1873365595

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113389039_113389040delinsTG , CM000671.2:g.113389039_113389040delinsTG	GRCh38
NC_000009.11:g.116151319_116151320delinsTG , CM000671.1:g.116151319_116151320delinsTG	GRCh37
NC_000009.10:g.115191140_115191141delinsTG	NCBI36
NG_008716.1:g.17299_17300delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.868_869delinsCA MANE Select	ENSP00000386284.3:p.Gln290=
ENST00000409155.7:c.868_869delinsCA	ENSP00000386284.3:p.Gln290=
ENST00000482847.5:n.1141_1142delinsCA
NM_000031.5:c.868_869delinsCA	NP_000022.3:p.Gln290=
XM_005251799.1:c.955_956delinsCA	XP_005251856.1:p.Gln319=
XM_011518363.1:c.994_995delinsCA	XP_011516665.1:p.Gln332=
XM_011518364.1:c.895_896delinsCA	XP_011516666.1:p.Gln299=
NM_001003945.2:c.955_956delinsCA	NP_001003945.1:p.Gln319=
NM_001317745.1:c.844_845delinsCA	NP_001304674.1:p.Gln282=
XM_011518364.2:c.895_896delinsCA	XP_011516666.1:p.Gln299=
XM_024447449.1:c.955_956delinsCA	XP_024303217.1:p.Gln319=
NM_000031.6:c.868_869delinsCA MANE Select	NP_000022.3:p.Gln290=
NM_001003945.3:c.955_956delinsCA	NP_001003945.1:p.Gln319=
NM_001317745.2:c.844_845delinsCA	NP_001304674.1:p.Gln282=