Canonical Allele Identifier: CA2673072217
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213378_1213379insCCA , CM000667.2:g.1213378_1213379insCCA GRCh38
NC_000005.9:g.1213493_1213494insCCA , CM000667.1:g.1213493_1213494insCCA GRCh37
NC_000005.8:g.1266493_1266494insCCA NCBI36
NG_008282.1:g.16784_16785insCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-85_664-84insCCA MANE Select ENSP00000305302.10:n.664-85_664-84insCCA
ENST00000304460.10:c.664-85_664-84insCCA ENSP00000305302.10:n.664-85_664-84insCCA
ENST00000515652.5:c.572-85_572-84insCCA ENSP00000425701.1:n.572-85_572-84insCCA
NM_001003841.2:c.664-85_664-84insCCA NP_001003841.1:n.664-85_664-84insCCA
NM_001003841.3:c.664-85_664-84insCCA MANE Select NP_001003841.1:n.664-85_664-84insCCA