Canonical Allele Identifier: CA2578258875
Gene: SLC6A19 HGNC NCBI

Linked Data

gnomAD v4: 5-1213373-G-GC

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213378dup , CM000667.2:g.1213378dup GRCh38
NC_000005.9:g.1213493dup , CM000667.1:g.1213493dup GRCh37
NC_000005.8:g.1266493dup NCBI36
NG_008282.1:g.16784dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-85dup MANE Select ENSP00000305302.10:n.664-85dup
ENST00000304460.10:c.664-85dup ENSP00000305302.10:n.664-85dup
ENST00000515652.5:c.572-85dup ENSP00000425701.1:n.572-85dup
NM_001003841.2:c.664-85dup NP_001003841.1:n.664-85dup
NM_001003841.3:c.664-85dup MANE Select NP_001003841.1:n.664-85dup