Canonical Allele Identifier: CA1522519489
Gene: SLC6A19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.1212955_1212956delinsGC , CM000667.2:g.1212955_1212956delinsGC GRCh38
NC_000005.9:g.1213070_1213071delinsGC , CM000667.1:g.1213070_1213071delinsGC GRCh37
NC_000005.8:g.1266070_1266071delinsGC NCBI36
NG_008282.1:g.16361_16362delinsGC

Transcript Alleles

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