Canonical Allele Identifier: CA2765038634
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213093dup , CM000667.2:g.1213093dup GRCh38
NC_000005.9:g.1213208dup , CM000667.1:g.1213208dup GRCh37
NC_000005.8:g.1266208dup NCBI36
NG_008282.1:g.16499dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-370dup MANE Select ENSP00000305302.10:n.664-370dup
ENST00000304460.10:c.664-370dup ENSP00000305302.10:n.664-370dup
ENST00000515652.5:c.572-370dup ENSP00000425701.1:n.572-370dup
NM_001003841.2:c.664-370dup NP_001003841.1:n.664-370dup
NM_001003841.3:c.664-370dup MANE Select NP_001003841.1:n.664-370dup