Canonical Allele Identifier: CA2695035933

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688517-ACCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688523_153688525del , CM000685.2:g.153688523_153688525del	GRCh38
NC_000023.10:g.152953978_152953980del , CM000685.1:g.152953978_152953980del	GRCh37
NC_000023.9:g.152607172_152607174del	NCBI36
NG_012016.1:g.5227_5229del
NG_012016.2:g.5227_5229del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.-52_-50del (SLC6A8) MANE Select	ENSP00000253122.5:n.-52_-50del
ENST00000253122.9:c.-52_-50del (SLC6A8)	ENSP00000253122.5:n.-52_-50del
ENST00000458354.5:c.-3+295_-3+297del (PNCK)	ENSP00000401542.1:n.-3+295_-3+297del
ENST00000480693.1:n.64+295_64+297del (PNCK)
NM_001142805.1:c.-52_-50del (SLC6A8)	NP_001136277.1:n.-52_-50del
NM_005629.3:c.-52_-50del (SLC6A8)	NP_005620.1:n.-52_-50del
NM_005629.4:c.-52_-50del (SLC6A8) MANE Select	NP_005620.1:n.-52_-50del
NM_001142805.2:c.-52_-50del (SLC6A8)	NP_001136277.1:n.-52_-50del