Canonical Allele Identifier: CA2765038635
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213097del , CM000667.2:g.1213097del GRCh38
NC_000005.9:g.1213212del , CM000667.1:g.1213212del GRCh37
NC_000005.8:g.1266212del NCBI36
NG_008282.1:g.16503del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-366del MANE Select ENSP00000305302.10:n.664-366del
ENST00000304460.10:c.664-366del ENSP00000305302.10:n.664-366del
ENST00000515652.5:c.572-366del ENSP00000425701.1:n.572-366del
NM_001003841.2:c.664-366del NP_001003841.1:n.664-366del
NM_001003841.3:c.664-366del MANE Select NP_001003841.1:n.664-366del