Canonical Allele Identifier: CA1522520317
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213526_1213527delinsAC , CM000667.2:g.1213526_1213527delinsAC GRCh38
NC_000005.9:g.1213641_1213642delinsAC , CM000667.1:g.1213641_1213642delinsAC GRCh37
NC_000005.8:g.1266641_1266642delinsAC NCBI36
NG_008282.1:g.16932_16933delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000304460.11:c.727_728delinsAC MANE Select ENSP00000305302.10:p.Thr243=
ENST00000304460.10:c.727_728delinsAC ENSP00000305302.10:p.Thr243=
ENST00000515652.5:c.635_636delinsAC ENSP00000425701.1:p.Asp212=
NM_001003841.2:c.727_728delinsAC NP_001003841.1:p.Thr243=
NM_001003841.3:c.727_728delinsAC MANE Select NP_001003841.1:p.Thr243=