Canonical Allele Identifier: CA2695036035

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688541-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688542dup , CM000685.2:g.153688542dup	GRCh38
NC_000023.10:g.152953997dup , CM000685.1:g.152953997dup	GRCh37
NC_000023.9:g.152607191dup	NCBI36
NG_012016.1:g.5246dup
NG_012016.2:g.5246dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.-33dup (SLC6A8) MANE Select	ENSP00000253122.5:n.-33dup
ENST00000253122.9:c.-33dup (SLC6A8)	ENSP00000253122.5:n.-33dup
ENST00000458354.5:c.-3+273dup (PNCK)	ENSP00000401542.1:n.-3+273dup
ENST00000480693.1:n.64+273dup (PNCK)
NM_001142805.1:c.-33dup (SLC6A8)	NP_001136277.1:n.-33dup
NM_005629.3:c.-33dup (SLC6A8)	NP_005620.1:n.-33dup
NM_005629.4:c.-33dup (SLC6A8) MANE Select	NP_005620.1:n.-33dup
NM_001142805.2:c.-33dup (SLC6A8)	NP_001136277.1:n.-33dup