Canonical Allele Identifier: CA2673072080
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213341_1213393del , CM000667.2:g.1213341_1213393del GRCh38
NC_000005.9:g.1213456_1213508del , CM000667.1:g.1213456_1213508del GRCh37
NC_000005.8:g.1266456_1266508del NCBI36
NG_008282.1:g.16747_16799del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-122_664-70del MANE Select ENSP00000305302.10:n.664-122_664-70del
ENST00000304460.10:c.664-122_664-70del ENSP00000305302.10:n.664-122_664-70del
ENST00000515652.5:c.572-122_572-70del ENSP00000425701.1:n.572-122_572-70del
NM_001003841.2:c.664-122_664-70del NP_001003841.1:n.664-122_664-70del
NM_001003841.3:c.664-122_664-70del MANE Select NP_001003841.1:n.664-122_664-70del