Canonical Allele Identifier: CA2673072136
Gene: SLC6A19 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1213356_1213357insCA , CM000667.2:g.1213356_1213357insCA GRCh38
NC_000005.9:g.1213471_1213472insCA , CM000667.1:g.1213471_1213472insCA GRCh37
NC_000005.8:g.1266471_1266472insCA NCBI36
NG_008282.1:g.16762_16763insCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.664-107_664-106insCA MANE Select ENSP00000305302.10:n.664-107_664-106insCA
ENST00000304460.10:c.664-107_664-106insCA ENSP00000305302.10:n.664-107_664-106insCA
ENST00000515652.5:c.572-107_572-106insCA ENSP00000425701.1:n.572-107_572-106insCA
NM_001003841.2:c.664-107_664-106insCA NP_001003841.1:n.664-107_664-106insCA
NM_001003841.3:c.664-107_664-106insCA MANE Select NP_001003841.1:n.664-107_664-106insCA