Canonical Allele Identifier: CA1072491872
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212967_1212969del , CM000667.2:g.1212967_1212969del GRCh38
NC_000005.9:g.1213082_1213084del , CM000667.1:g.1213082_1213084del GRCh37
NC_000005.8:g.1266082_1266084del NCBI36
NG_008282.1:g.16373_16375del

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.663+483_663+485del MANE Select ENSP00000305302.10:n.663+483_663+485del
ENST00000304460.10:c.663+483_663+485del ENSP00000305302.10:n.663+483_663+485del
ENST00000515652.5:c.571+483_571+485del ENSP00000425701.1:n.571+483_571+485del
NM_001003841.2:c.663+483_663+485del NP_001003841.1:n.663+483_663+485del
NM_001003841.3:c.663+483_663+485del MANE Select NP_001003841.1:n.663+483_663+485del