Canonical Allele Identifier: CA2673072165
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213371_1213416del , CM000667.2:g.1213371_1213416del GRCh38
NC_000005.9:g.1213486_1213531del , CM000667.1:g.1213486_1213531del GRCh37
NC_000005.8:g.1266486_1266531del NCBI36
NG_008282.1:g.16777_16822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-92_664-47del MANE Select ENSP00000305302.10:n.664-92_664-47del
ENST00000304460.10:c.664-92_664-47del ENSP00000305302.10:n.664-92_664-47del
ENST00000515652.5:c.572-92_572-47del ENSP00000425701.1:n.572-92_572-47del
NM_001003841.2:c.664-92_664-47del NP_001003841.1:n.664-92_664-47del
NM_001003841.3:c.664-92_664-47del MANE Select NP_001003841.1:n.664-92_664-47del