Canonical Allele Identifier: CA1522519583
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213032_1213033delinsAC , CM000667.2:g.1213032_1213033delinsAC GRCh38
NC_000005.9:g.1213147_1213148delinsAC , CM000667.1:g.1213147_1213148delinsAC GRCh37
NC_000005.8:g.1266147_1266148delinsAC NCBI36
NG_008282.1:g.16438_16439delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-431_664-430delinsAC MANE Select ENSP00000305302.10:n.664-431_664-430delinsAC
ENST00000304460.10:c.664-431_664-430delinsAC ENSP00000305302.10:n.664-431_664-430delinsAC
ENST00000515652.5:c.572-431_572-430delinsAC ENSP00000425701.1:n.572-431_572-430delinsAC
NM_001003841.2:c.664-431_664-430delinsAC NP_001003841.1:n.664-431_664-430delinsAC
NM_001003841.3:c.664-431_664-430delinsAC MANE Select NP_001003841.1:n.664-431_664-430delinsAC