Canonical Allele Identifier: CA1522520619
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213791G= , CM000667.2:g.1213791G= GRCh38
NC_000005.9:g.1213906G= , CM000667.1:g.1213906G= GRCh37
NC_000005.8:g.1266906G= NCBI36
NG_008282.1:g.17197G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.775-162G= MANE Select ENSP00000305302.10:n.775-162G=
ENST00000304460.10:c.775-162G= ENSP00000305302.10:n.775-162G=
ENST00000515652.5:c.683-162G= ENSP00000425701.1:n.683-162G=
NM_001003841.2:c.775-162G= NP_001003841.1:n.775-162G=
NM_001003841.3:c.775-162G= MANE Select NP_001003841.1:n.775-162G=