Canonical Allele Identifier: CA2695035808

Gene: SLC6A8 PNCK

Linked Data

• gnomAD v4: X-153688462-CCGGCCGGCCCGCGCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.153688466_153688482del , CM000685.2:g.153688466_153688482del	GRCh38
NC_000023.10:g.152953921_152953937del , CM000685.1:g.152953921_152953937del	GRCh37
NC_000023.9:g.152607115_152607131del	NCBI36
NG_012016.1:g.5170_5186del
NG_012016.2:g.5170_5186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000253122.10:c.-109_-93del (SLC6A8) MANE Select	ENSP00000253122.5:n.-109_-93del
ENST00000253122.9:c.-109_-93del (SLC6A8)	ENSP00000253122.5:n.-109_-93del
ENST00000458354.5:c.-3+336_-3+352del (PNCK)	ENSP00000401542.1:n.-3+336_-3+352del
ENST00000480693.1:n.64+336_64+352del (PNCK)
NM_001142805.1:c.-109_-93del (SLC6A8)	NP_001136277.1:n.-109_-93del
NM_005629.3:c.-109_-93del (SLC6A8)	NP_005620.1:n.-109_-93del
NM_005629.4:c.-109_-93del (SLC6A8) MANE Select	NP_005620.1:n.-109_-93del
NM_001142805.2:c.-109_-93del (SLC6A8)	NP_001136277.1:n.-109_-93del