Canonical Allele Identifier: CA2840003527

Gene: SLC6A8 PNCK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688883_153688884insGCGGGG , CM000685.2:g.153688883_153688884insGCGGGG	GRCh38
NC_000023.10:g.152954338_152954339insGCGGGG , CM000685.1:g.152954338_152954339insGCGGGG	GRCh37
NC_000023.9:g.152607532_152607533insGCGGGG	NCBI36
NG_012016.1:g.5587_5588insGCGGGG
NG_012016.2:g.5587_5588insGCGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.262+47_262+48insGCGGGG (SLC6A8) MANE Select	ENSP00000253122.5:n.262+47_262+48insGCGGGG
ENST00000253122.9:c.262+47_262+48insGCGGGG (SLC6A8)	ENSP00000253122.5:n.262+47_262+48insGCGGGG
ENST00000458354.5:c.-70_-69insCCGCCC (PNCK)	ENSP00000401542.1:n.-70_-69insCCGCCC
ENST00000476466.1:n.114+47_114+48insGCGGGG (SLC6A8)
NM_001142805.1:c.262+47_262+48insGCGGGG (SLC6A8)	NP_001136277.1:n.262+47_262+48insGCGGGG
NM_005629.3:c.262+47_262+48insGCGGGG (SLC6A8)	NP_005620.1:n.262+47_262+48insGCGGGG
NM_005629.4:c.262+47_262+48insGCGGGG (SLC6A8) MANE Select	NP_005620.1:n.262+47_262+48insGCGGGG
NM_001142805.2:c.262+47_262+48insGCGGGG (SLC6A8)	NP_001136277.1:n.262+47_262+48insGCGGGG