Canonical Allele Identifier: CA2673072239
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213392_1213437del , CM000667.2:g.1213392_1213437del GRCh38
NC_000005.9:g.1213507_1213552del , CM000667.1:g.1213507_1213552del GRCh37
NC_000005.8:g.1266507_1266552del NCBI36
NG_008282.1:g.16798_16843del

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.664-71_664-26del MANE Select ENSP00000305302.10:n.664-71_664-26del
ENST00000304460.10:c.664-71_664-26del ENSP00000305302.10:n.664-71_664-26del
ENST00000515652.5:c.572-71_572-26del ENSP00000425701.1:n.572-71_572-26del
NM_001003841.2:c.664-71_664-26del NP_001003841.1:n.664-71_664-26del
NM_001003841.3:c.664-71_664-26del MANE Select NP_001003841.1:n.664-71_664-26del