Canonical Allele Identifier: CA2579744112

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688887-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688887C>A , CM000685.2:g.153688887C>A	GRCh38
NC_000023.10:g.152954342C>A , CM000685.1:g.152954342C>A	GRCh37
NC_000023.9:g.152607536C>A	NCBI36
NG_012016.1:g.5591C>A
NG_012016.2:g.5591C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.262+51C>A (SLC6A8) MANE Select	ENSP00000253122.5:n.262+51C>A
ENST00000253122.9:c.262+51C>A (SLC6A8)	ENSP00000253122.5:n.262+51C>A
ENST00000458354.5:c.-75G>T (PNCK)	ENSP00000401542.1:n.-75G>T
ENST00000476466.1:n.114+51C>A (SLC6A8)
NM_001142805.1:c.262+51C>A (SLC6A8)	NP_001136277.1:n.262+51C>A
NM_005629.3:c.262+51C>A (SLC6A8)	NP_005620.1:n.262+51C>A
NM_005629.4:c.262+51C>A (SLC6A8) MANE Select	NP_005620.1:n.262+51C>A
NM_001142805.2:c.262+51C>A (SLC6A8)	NP_001136277.1:n.262+51C>A