Canonical Allele Identifier: CA2552314008

Gene: SLC6A19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1213830dup , CM000667.2:g.1213830dup	GRCh38
NC_000005.9:g.1213945dup , CM000667.1:g.1213945dup	GRCh37
NC_000005.8:g.1266945dup	NCBI36
NG_008282.1:g.17236dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.775-123dup MANE Select	ENSP00000305302.10:n.775-123dup
ENST00000304460.10:c.775-123dup	ENSP00000305302.10:n.775-123dup
ENST00000515652.5:c.683-123dup	ENSP00000425701.1:n.683-123dup
NM_001003841.2:c.775-123dup	NP_001003841.1:n.775-123dup
NM_001003841.3:c.775-123dup MANE Select	NP_001003841.1:n.775-123dup