Canonical Allele Identifier: CA1522519593
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213045A= , CM000667.2:g.1213045A= GRCh38
NC_000005.9:g.1213160A= , CM000667.1:g.1213160A= GRCh37
NC_000005.8:g.1266160A= NCBI36
NG_008282.1:g.16451A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-418A= MANE Select ENSP00000305302.10:n.664-418A=
ENST00000304460.10:c.664-418A= ENSP00000305302.10:n.664-418A=
ENST00000515652.5:c.572-418A= ENSP00000425701.1:n.572-418A=
NM_001003841.2:c.664-418A= NP_001003841.1:n.664-418A=
NM_001003841.3:c.664-418A= MANE Select NP_001003841.1:n.664-418A=