Canonical Allele Identifier: CA2466435916

Gene: SLC6A8 PNCK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688842T= , CM000685.2:g.153688842T=	GRCh38
NC_000023.10:g.152954297T= , CM000685.1:g.152954297T=	GRCh37
NC_000023.9:g.152607491T=	NCBI36
NG_012016.1:g.5546T=
NG_012016.2:g.5546T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000253122.10:c.262+6T= (SLC6A8) MANE Select	ENSP00000253122.5:n.262+6T=
ENST00000253122.9:c.262+6T= (SLC6A8)	ENSP00000253122.5:n.262+6T=
ENST00000458354.5:c.-30A= (PNCK)	ENSP00000401542.1:n.-30A=
ENST00000476466.1:n.114+6T= (SLC6A8)
ENST00000480693.1:n.37A= (PNCK)
NM_001142805.1:c.262+6T= (SLC6A8)	NP_001136277.1:n.262+6T=
NM_005629.3:c.262+6T= (SLC6A8)	NP_005620.1:n.262+6T=
NM_005629.4:c.262+6T= (SLC6A8) MANE Select	NP_005620.1:n.262+6T=
NM_001142805.2:c.262+6T= (SLC6A8)	NP_001136277.1:n.262+6T=