Canonical Allele Identifier: CA2673072393
Gene: SLC6A19 HGNC NCBI

Linked Data

gnomAD v4: 5-1213709-TC-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213711del , CM000667.2:g.1213711del GRCh38
NC_000005.9:g.1213826del , CM000667.1:g.1213826del GRCh37
NC_000005.8:g.1266826del NCBI36
NG_008282.1:g.17117del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.774+138del MANE Select ENSP00000305302.10:n.774+138del
ENST00000304460.10:c.774+138del ENSP00000305302.10:n.774+138del
ENST00000515652.5:c.682+138del ENSP00000425701.1:n.682+138del
NM_001003841.2:c.774+138del NP_001003841.1:n.774+138del
NM_001003841.3:c.774+138del MANE Select NP_001003841.1:n.774+138del