Canonical Allele Identifier: CA415076192

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688660-G-T
• MyVariant Identifiers: chrX:g.152954115G>T (hg19) ; chrX:g.153688660G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688660G>T , CM000685.2:g.153688660G>T	GRCh38
NC_000023.10:g.152954115G>T , CM000685.1:g.152954115G>T	GRCh37
NC_000023.9:g.152607309G>T	NCBI36
NG_012016.1:g.5364G>T
NG_012016.2:g.5364G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.86G>T (SLC6A8) MANE Select	ENSP00000253122.5:p.Gly29Val
ENST00000253122.9:c.86G>T (SLC6A8)	ENSP00000253122.5:p.Gly29Val
ENST00000458354.5:c.-3+155C>A (PNCK)	ENSP00000401542.1:n.-3+155C>A
ENST00000480693.1:n.64+155C>A (PNCK)
NM_001142805.1:c.86G>T (SLC6A8)	NP_001136277.1:p.Gly29Val
NM_005629.3:c.86G>T (SLC6A8)	NP_005620.1:p.Gly29Val
NM_005629.4:c.86G>T (SLC6A8) MANE Select	NP_005620.1:p.Gly29Val
NM_001142805.2:c.86G>T (SLC6A8)	NP_001136277.1:p.Gly29Val