Canonical Allele Identifier: CA2765038616
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212955_1212956insGGG , CM000667.2:g.1212955_1212956insGGG GRCh38
NC_000005.9:g.1213070_1213071insGGG , CM000667.1:g.1213070_1213071insGGG GRCh37
NC_000005.8:g.1266070_1266071insGGG NCBI36
NG_008282.1:g.16361_16362insGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000304460.11:c.663+471_663+472insGGG MANE Select ENSP00000305302.10:n.663+471_663+472insGGG
ENST00000304460.10:c.663+471_663+472insGGG ENSP00000305302.10:n.663+471_663+472insGGG
ENST00000515652.5:c.571+471_571+472insGGG ENSP00000425701.1:n.571+471_571+472insGGG
NM_001003841.2:c.663+471_663+472insGGG NP_001003841.1:n.663+471_663+472insGGG
NM_001003841.3:c.663+471_663+472insGGG MANE Select NP_001003841.1:n.663+471_663+472insGGG