Canonical Allele Identifier: CA1522520739

Gene: SLC6A19

Linked Data

• dbSNP Id: rs1746125461

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1213889_1213891del , CM000667.2:g.1213889_1213891del	GRCh38
NC_000005.9:g.1214004_1214006del , CM000667.1:g.1214004_1214006del	GRCh37
NC_000005.8:g.1267004_1267006del	NCBI36
NG_008282.1:g.17295_17297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.775-64_775-62del MANE Select	ENSP00000305302.10:n.775-64_775-62del
ENST00000304460.10:c.775-64_775-62del	ENSP00000305302.10:n.775-64_775-62del
ENST00000515652.5:c.683-64_683-62del	ENSP00000425701.1:n.683-64_683-62del
NM_001003841.2:c.775-64_775-62del	NP_001003841.1:n.775-64_775-62del
NM_001003841.3:c.775-64_775-62del MANE Select	NP_001003841.1:n.775-64_775-62del