Canonical Allele Identifier: CA2526995118

Gene: SLC6A19

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.1212965dup , CM000667.2:g.1212965dup	GRCh38
NC_000005.9:g.1213080dup , CM000667.1:g.1213080dup	GRCh37
NC_000005.8:g.1266080dup	NCBI36
NG_008282.1:g.16371dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000304460.11:c.663+481dup MANE Select	ENSP00000305302.10:n.663+481dup
ENST00000304460.10:c.663+481dup	ENSP00000305302.10:n.663+481dup
ENST00000515652.5:c.571+481dup	ENSP00000425701.1:n.571+481dup
NM_001003841.2:c.663+481dup	NP_001003841.1:n.663+481dup
NM_001003841.3:c.663+481dup MANE Select	NP_001003841.1:n.663+481dup