Canonical Allele Identifier: CA1522520069
Gene: SLC6A19 HGNC NCBI

Linked Data

dbSNP Id: rs1746104659

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213394_1213395insTGTGCCCCGCCCCCA , CM000667.2:g.1213394_1213395insTGTGCCCCGCCCCCA GRCh38
NC_000005.9:g.1213509_1213510insTGTGCCCCGCCCCCA , CM000667.1:g.1213509_1213510insTGTGCCCCGCCCCCA GRCh37
NC_000005.8:g.1266509_1266510insTGTGCCCCGCCCCCA NCBI36
NG_008282.1:g.16800_16801insTGTGCCCCGCCCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-69_664-68insTGTGCCCCGCCCCCA MANE Select ENSP00000305302.10:n.664-69_664-68insTGTGCCCCGCCCCCA
ENST00000304460.10:c.664-69_664-68insTGTGCCCCGCCCCCA ENSP00000305302.10:n.664-69_664-68insTGTGCCCCGCCCCCA
ENST00000515652.5:c.572-69_572-68insTGTGCCCCGCCCCCA ENSP00000425701.1:n.572-69_572-68insTGTGCCCCGCCCCCA
NM_001003841.2:c.664-69_664-68insTGTGCCCCGCCCCCA NP_001003841.1:n.664-69_664-68insTGTGCCCCGCCCCCA
NM_001003841.3:c.664-69_664-68insTGTGCCCCGCCCCCA MANE Select NP_001003841.1:n.664-69_664-68insTGTGCCCCGCCCCCA