Canonical Allele Identifier: CA2765038657
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213230_1213406del , CM000667.2:g.1213230_1213406del GRCh38
NC_000005.9:g.1213345_1213521del , CM000667.1:g.1213345_1213521del GRCh37
NC_000005.8:g.1266345_1266521del NCBI36
NG_008282.1:g.16636_16812del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-233_664-57del MANE Select ENSP00000305302.10:n.664-233_664-57del
ENST00000304460.10:c.664-233_664-57del ENSP00000305302.10:n.664-233_664-57del
ENST00000515652.5:c.572-233_572-57del ENSP00000425701.1:n.572-233_572-57del
NM_001003841.2:c.664-233_664-57del NP_001003841.1:n.664-233_664-57del
NM_001003841.3:c.664-233_664-57del MANE Select NP_001003841.1:n.664-233_664-57del