Canonical Allele Identifier: CA2740609830
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213827_1213828insT , CM000667.2:g.1213827_1213828insT GRCh38
NC_000005.9:g.1213942_1213943insT , CM000667.1:g.1213942_1213943insT GRCh37
NC_000005.8:g.1266942_1266943insT NCBI36
NG_008282.1:g.17233_17234insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.775-126_775-125insT MANE Select ENSP00000305302.10:n.775-126_775-125insT
ENST00000304460.10:c.775-126_775-125insT ENSP00000305302.10:n.775-126_775-125insT
ENST00000515652.5:c.683-126_683-125insT ENSP00000425701.1:n.683-126_683-125insT
NM_001003841.2:c.775-126_775-125insT NP_001003841.1:n.775-126_775-125insT
NM_001003841.3:c.775-126_775-125insT MANE Select NP_001003841.1:n.775-126_775-125insT