Canonical Allele Identifier: CA2695037539

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688915-GGGT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688917_153688919del , CM000685.2:g.153688917_153688919del	GRCh38
NC_000023.10:g.152954372_152954374del , CM000685.1:g.152954372_152954374del	GRCh37
NC_000023.9:g.152607566_152607568del	NCBI36
NG_012016.1:g.5621_5623del
NG_012016.2:g.5621_5623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.262+81_262+83del (SLC6A8) MANE Select	ENSP00000253122.5:n.262+81_262+83del
ENST00000253122.9:c.262+81_262+83del (SLC6A8)	ENSP00000253122.5:n.262+81_262+83del
ENST00000458354.5:c.-106_-104del (PNCK)	ENSP00000401542.1:n.-106_-104del
ENST00000476466.1:n.114+81_114+83del (SLC6A8)
NM_001142805.1:c.262+81_262+83del (SLC6A8)	NP_001136277.1:n.262+81_262+83del
NM_005629.3:c.262+81_262+83del (SLC6A8)	NP_005620.1:n.262+81_262+83del
NM_005629.4:c.262+81_262+83del (SLC6A8) MANE Select	NP_005620.1:n.262+81_262+83del
NM_001142805.2:c.262+81_262+83del (SLC6A8)	NP_001136277.1:n.262+81_262+83del