Canonical Allele Identifier: CA2578258895
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213421_1213422insT , CM000667.2:g.1213421_1213422insT GRCh38
NC_000005.9:g.1213536_1213537insT , CM000667.1:g.1213536_1213537insT GRCh37
NC_000005.8:g.1266536_1266537insT NCBI36
NG_008282.1:g.16827_16828insT

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.664-42_664-41insT MANE Select ENSP00000305302.10:n.664-42_664-41insT
ENST00000304460.10:c.664-42_664-41insT ENSP00000305302.10:n.664-42_664-41insT
ENST00000515652.5:c.572-42_572-41insT ENSP00000425701.1:n.572-42_572-41insT
NM_001003841.2:c.664-42_664-41insT NP_001003841.1:n.664-42_664-41insT
NM_001003841.3:c.664-42_664-41insT MANE Select NP_001003841.1:n.664-42_664-41insT