Canonical Allele Identifier: CA1072491886
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212973_1212975del , CM000667.2:g.1212973_1212975del GRCh38
NC_000005.9:g.1213088_1213090del , CM000667.1:g.1213088_1213090del GRCh37
NC_000005.8:g.1266088_1266090del NCBI36
NG_008282.1:g.16379_16381del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-490_664-488del MANE Select ENSP00000305302.10:n.664-490_664-488del
ENST00000304460.10:c.664-490_664-488del ENSP00000305302.10:n.664-490_664-488del
ENST00000515652.5:c.572-490_572-488del ENSP00000425701.1:n.572-490_572-488del
NM_001003841.2:c.664-490_664-488del NP_001003841.1:n.664-490_664-488del
NM_001003841.3:c.664-490_664-488del MANE Select NP_001003841.1:n.664-490_664-488del