Canonical Allele Identifier: CA1873365462

Gene: ALAD

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.113388787_113388789delinsGCT , CM000671.2:g.113388787_113388789delinsGCT	GRCh38
NC_000009.11:g.116151067_116151069delinsGCT , CM000671.1:g.116151067_116151069delinsGCT	GRCh37
NC_000009.10:g.115190888_115190890delinsGCT	NCBI36
NG_008716.1:g.17550_17552delinsAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409155.8:c.931+188_931+190delinsAGC MANE Select	ENSP00000386284.3:n.931+188_931+190delinsAGC
ENST00000409155.7:c.931+188_931+190delinsAGC	ENSP00000386284.3:n.931+188_931+190delinsAGC
ENST00000482847.5:n.1204+188_1204+190delinsAGC
NM_000031.5:c.931+188_931+190delinsAGC	NP_000022.3:n.931+188_931+190delinsAGC
XM_005251799.1:c.1018+188_1018+190delinsAGC	XP_005251856.1:n.1018+188_1018+190delinsAGC
XM_011518363.1:c.1057+188_1057+190delinsAGC	XP_011516665.1:n.1057+188_1057+190delinsAGC
XM_011518364.1:c.958+188_958+190delinsAGC	XP_011516666.1:n.958+188_958+190delinsAGC
NM_001003945.2:c.1018+188_1018+190delinsAGC	NP_001003945.1:n.1018+188_1018+190delinsAGC
NM_001317745.1:c.907+188_907+190delinsAGC	NP_001304674.1:n.907+188_907+190delinsAGC
XM_011518364.2:c.958+188_958+190delinsAGC	XP_011516666.1:n.958+188_958+190delinsAGC
XM_024447449.1:c.1018+188_1018+190delinsAGC	XP_024303217.1:n.1018+188_1018+190delinsAGC
NM_000031.6:c.931+188_931+190delinsAGC MANE Select	NP_000022.3:n.931+188_931+190delinsAGC
NM_001003945.3:c.1018+188_1018+190delinsAGC	NP_001003945.1:n.1018+188_1018+190delinsAGC
NM_001317745.2:c.907+188_907+190delinsAGC	NP_001304674.1:n.907+188_907+190delinsAGC