Canonical Allele Identifier: CA2673072145
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213357_1213358insAC , CM000667.2:g.1213357_1213358insAC GRCh38
NC_000005.9:g.1213472_1213473insAC , CM000667.1:g.1213472_1213473insAC GRCh37
NC_000005.8:g.1266472_1266473insAC NCBI36
NG_008282.1:g.16763_16764insAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-106_664-105insAC MANE Select ENSP00000305302.10:n.664-106_664-105insAC
ENST00000304460.10:c.664-106_664-105insAC ENSP00000305302.10:n.664-106_664-105insAC
ENST00000515652.5:c.572-106_572-105insAC ENSP00000425701.1:n.572-106_572-105insAC
NM_001003841.2:c.664-106_664-105insAC NP_001003841.1:n.664-106_664-105insAC
NM_001003841.3:c.664-106_664-105insAC MANE Select NP_001003841.1:n.664-106_664-105insAC