Canonical Allele Identifier: CA359060019
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1201708G>A , CM000667.2:g.1201708G>A GRCh38
NC_000005.9:g.1201823G>A , CM000667.1:g.1201823G>A GRCh37
NC_000005.8:g.1254823G>A NCBI36
NG_008282.1:g.5114G>A

Transcript Alleles

HGVS Amino-acid Change
NM_001003841.3:c.58G>A MANE Select NP_001003841.1:p.Glu20Lys
ENST00000304460.11:c.58G>A MANE Select ENSP00000305302.10:p.Glu20Lys
NM_001003841.2:c.58G>A NP_001003841.1:p.Glu20Lys
ENST00000304460.10:c.58G>A ENSP00000305302.10:p.Glu20Lys
ENST00000515652.5:c.58G>A ENSP00000425701.1:p.Glu20Lys