Canonical Allele Identifier: CA2673072154
Gene: SLC6A19 HGNC NCBI

Linked Data

gnomAD v4: 5-1213359-TC-T

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213363del , CM000667.2:g.1213363del GRCh38
NC_000005.9:g.1213478del , CM000667.1:g.1213478del GRCh37
NC_000005.8:g.1266478del NCBI36
NG_008282.1:g.16769del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-100del MANE Select ENSP00000305302.10:n.664-100del
ENST00000304460.10:c.664-100del ENSP00000305302.10:n.664-100del
ENST00000515652.5:c.572-100del ENSP00000425701.1:n.572-100del
NM_001003841.2:c.664-100del NP_001003841.1:n.664-100del
NM_001003841.3:c.664-100del MANE Select NP_001003841.1:n.664-100del