Canonical Allele Identifier: CA1522519547
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212990T= , CM000667.2:g.1212990T= GRCh38
NC_000005.9:g.1213105T= , CM000667.1:g.1213105T= GRCh37
NC_000005.8:g.1266105T= NCBI36
NG_008282.1:g.16396T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-473T= MANE Select ENSP00000305302.10:n.664-473T=
ENST00000304460.10:c.664-473T= ENSP00000305302.10:n.664-473T=
ENST00000515652.5:c.572-473T= ENSP00000425701.1:n.572-473T=
NM_001003841.2:c.664-473T= NP_001003841.1:n.664-473T=
NM_001003841.3:c.664-473T= MANE Select NP_001003841.1:n.664-473T=