Canonical Allele Identifier: CA519344416

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688784-G-T
• MyVariant Identifiers: chrX:g.152954239G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688784G>T , CM000685.2:g.153688784G>T	GRCh38
NC_000023.10:g.152954239G>T , CM000685.1:g.152954239G>T	GRCh37
NC_000023.9:g.152607433G>T	NCBI36
NG_012016.1:g.5488G>T
NG_012016.2:g.5488G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.210G>T (SLC6A8) MANE Select	ENSP00000253122.5:p.Val70=
ENST00000253122.9:c.210G>T (SLC6A8)	ENSP00000253122.5:p.Val70=
ENST00000458354.5:c.-3+31C>A (PNCK)	ENSP00000401542.1:n.-3+31C>A
ENST00000476466.1:n.62G>T (SLC6A8)
ENST00000480693.1:n.64+31C>A (PNCK)
NM_001142805.1:c.210G>T (SLC6A8)	NP_001136277.1:p.Val70=
NM_005629.3:c.210G>T (SLC6A8)	NP_005620.1:p.Val70=
NM_005629.4:c.210G>T (SLC6A8) MANE Select	NP_005620.1:p.Val70=
NM_001142805.2:c.210G>T (SLC6A8)	NP_001136277.1:p.Val70=