Canonical Allele Identifier: CA2466435759

Gene: SLC6A8 PNCK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688496G= , CM000685.2:g.153688496G=	GRCh38
NC_000023.10:g.152953951G= , CM000685.1:g.152953951G=	GRCh37
NC_000023.9:g.152607145G=	NCBI36
NG_012016.1:g.5200G=
NG_012016.2:g.5200G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.-79G= (SLC6A8) MANE Select	ENSP00000253122.5:n.-79G=
ENST00000253122.9:c.-79G= (SLC6A8)	ENSP00000253122.5:n.-79G=
ENST00000458354.5:c.-3+319C= (PNCK)	ENSP00000401542.1:n.-3+319C=
ENST00000480693.1:n.64+319C= (PNCK)
NM_001142805.1:c.-79G= (SLC6A8)	NP_001136277.1:n.-79G=
NM_005629.3:c.-79G= (SLC6A8)	NP_005620.1:n.-79G=
NM_005629.4:c.-79G= (SLC6A8) MANE Select	NP_005620.1:n.-79G=
NM_001142805.2:c.-79G= (SLC6A8)	NP_001136277.1:n.-79G=