Canonical Allele Identifier: CA337216826

Gene: SLC6A8 PNCK

Linked Data

• dbSNP Id: rs782807678
• gnomAD v2: X-152954350-C-T
• gnomAD v3: X-153688895-C-T
• gnomAD v4: X-153688895-C-T
• MyVariant Identifiers: chrX:g.152954350C>T (hg19) ; chrX:g.153688895C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688895C>T , CM000685.2:g.153688895C>T	GRCh38
NC_000023.10:g.152954350C>T , CM000685.1:g.152954350C>T	GRCh37
NC_000023.9:g.152607544C>T	NCBI36
NG_012016.1:g.5599C>T
NG_012016.2:g.5599C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.262+59C>T (SLC6A8) MANE Select	ENSP00000253122.5:n.262+59C>T
ENST00000253122.9:c.262+59C>T (SLC6A8)	ENSP00000253122.5:n.262+59C>T
ENST00000458354.5:c.-83G>A (PNCK)	ENSP00000401542.1:n.-83G>A
ENST00000476466.1:n.114+59C>T (SLC6A8)
NM_001142805.1:c.262+59C>T (SLC6A8)	NP_001136277.1:n.262+59C>T
NM_005629.3:c.262+59C>T (SLC6A8)	NP_005620.1:n.262+59C>T
NM_005629.4:c.262+59C>T (SLC6A8) MANE Select	NP_005620.1:n.262+59C>T
NM_001142805.2:c.262+59C>T (SLC6A8)	NP_001136277.1:n.262+59C>T