Canonical Allele Identifier: CA2695035961

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688523-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688529dup , CM000685.2:g.153688529dup	GRCh38
NC_000023.10:g.152953984dup , CM000685.1:g.152953984dup	GRCh37
NC_000023.9:g.152607178dup	NCBI36
NG_012016.1:g.5233dup
NG_012016.2:g.5233dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.-46dup (SLC6A8) MANE Select	ENSP00000253122.5:n.-46dup
ENST00000253122.9:c.-46dup (SLC6A8)	ENSP00000253122.5:n.-46dup
ENST00000458354.5:c.-3+291dup (PNCK)	ENSP00000401542.1:n.-3+291dup
ENST00000480693.1:n.64+291dup (PNCK)
NM_001142805.1:c.-46dup (SLC6A8)	NP_001136277.1:n.-46dup
NM_005629.3:c.-46dup (SLC6A8)	NP_005620.1:n.-46dup
NM_005629.4:c.-46dup (SLC6A8) MANE Select	NP_005620.1:n.-46dup
NM_001142805.2:c.-46dup (SLC6A8)	NP_001136277.1:n.-46dup