Canonical Allele Identifier: CA645287863

Gene: SLC6A8 PNCK

Linked Data

• dbSNP Id: rs1557043881
• gnomAD v2: X-152954320-T-C
• gnomAD v4: X-153688865-T-C
• MyVariant Identifiers: chrX:g.152954320T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688865T>C , CM000685.2:g.153688865T>C	GRCh38
NC_000023.10:g.152954320T>C , CM000685.1:g.152954320T>C	GRCh37
NC_000023.9:g.152607514T>C	NCBI36
NG_012016.1:g.5569T>C
NG_012016.2:g.5569T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.262+29T>C (SLC6A8) MANE Select	ENSP00000253122.5:n.262+29T>C
ENST00000253122.9:c.262+29T>C (SLC6A8)	ENSP00000253122.5:n.262+29T>C
ENST00000458354.5:c.-53A>G (PNCK)	ENSP00000401542.1:n.-53A>G
ENST00000476466.1:n.114+29T>C (SLC6A8)
ENST00000480693.1:n.14A>G (PNCK)
NM_001142805.1:c.262+29T>C (SLC6A8)	NP_001136277.1:n.262+29T>C
NM_005629.3:c.262+29T>C (SLC6A8)	NP_005620.1:n.262+29T>C
NM_005629.4:c.262+29T>C (SLC6A8) MANE Select	NP_005620.1:n.262+29T>C
NM_001142805.2:c.262+29T>C (SLC6A8)	NP_001136277.1:n.262+29T>C