Canonical Allele Identifier: CA2579744071

Gene: SLC6A8 PNCK

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688480C>T , CM000685.2:g.153688480C>T	GRCh38
NC_000023.10:g.152953935C>T , CM000685.1:g.152953935C>T	GRCh37
NC_000023.9:g.152607129C>T	NCBI36
NG_012016.1:g.5184C>T
NG_012016.2:g.5184C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.-95C>T (SLC6A8) MANE Select	ENSP00000253122.5:n.-95C>T
ENST00000253122.9:c.-95C>T (SLC6A8)	ENSP00000253122.5:n.-95C>T
ENST00000458354.5:c.-3+335G>A (PNCK)	ENSP00000401542.1:n.-3+335G>A
ENST00000480693.1:n.64+335G>A (PNCK)
NM_001142805.1:c.-95C>T (SLC6A8)	NP_001136277.1:n.-95C>T
NM_005629.3:c.-95C>T (SLC6A8)	NP_005620.1:n.-95C>T
NM_005629.4:c.-95C>T (SLC6A8) MANE Select	NP_005620.1:n.-95C>T
NM_001142805.2:c.-95C>T (SLC6A8)	NP_001136277.1:n.-95C>T