Canonical Allele Identifier: CA2673072148
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213359_1213395del , CM000667.2:g.1213359_1213395del GRCh38
NC_000005.9:g.1213474_1213510del , CM000667.1:g.1213474_1213510del GRCh37
NC_000005.8:g.1266474_1266510del NCBI36
NG_008282.1:g.16765_16801del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-104_664-68del MANE Select ENSP00000305302.10:n.664-104_664-68del
ENST00000304460.10:c.664-104_664-68del ENSP00000305302.10:n.664-104_664-68del
ENST00000515652.5:c.572-104_572-68del ENSP00000425701.1:n.572-104_572-68del
NM_001003841.2:c.664-104_664-68del NP_001003841.1:n.664-104_664-68del
NM_001003841.3:c.664-104_664-68del MANE Select NP_001003841.1:n.664-104_664-68del