Canonical Allele Identifier: CA2571778441
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213312_1213424del , CM000667.2:g.1213312_1213424del GRCh38
NC_000005.9:g.1213427_1213539del , CM000667.1:g.1213427_1213539del GRCh37
NC_000005.8:g.1266427_1266539del NCBI36
NG_008282.1:g.16718_16830del

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.664-151_664-39del MANE Select ENSP00000305302.10:n.664-151_664-39del
ENST00000304460.10:c.664-151_664-39del ENSP00000305302.10:n.664-151_664-39del
ENST00000515652.5:c.572-151_572-39del ENSP00000425701.1:n.572-151_572-39del
NM_001003841.2:c.664-151_664-39del NP_001003841.1:n.664-151_664-39del
NM_001003841.3:c.664-151_664-39del MANE Select NP_001003841.1:n.664-151_664-39del