Canonical Allele Identifier: CA1072492079
Gene: SLC6A19 HGNC NCBI

Linked Data

gnomAD v3: 5-1213026-A-AT
gnomAD v4: 5-1213026-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213027dup , CM000667.2:g.1213027dup GRCh38
NC_000005.9:g.1213142dup , CM000667.1:g.1213142dup GRCh37
NC_000005.8:g.1266142dup NCBI36
NG_008282.1:g.16433dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-436dup MANE Select ENSP00000305302.10:n.664-436dup
ENST00000304460.10:c.664-436dup ENSP00000305302.10:n.664-436dup
ENST00000515652.5:c.572-436dup ENSP00000425701.1:n.572-436dup
NM_001003841.2:c.664-436dup NP_001003841.1:n.664-436dup
NM_001003841.3:c.664-436dup MANE Select NP_001003841.1:n.664-436dup
Search 100 bp 5'
Search 100 bp 3'