Canonical Allele Identifier: CA5553382
Gene: MRPS16 HGNC NCBI
DNAJC9-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs766189513

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.73251807A>G , CM000672.2:g.73251807A>G GRCh38
NC_000010.10:g.75011565A>G , CM000672.1:g.75011565A>G GRCh37
NC_000010.9:g.74681571A>G NCBI36
NG_008096.1:g.5887T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000372945.8:c.230T>C (MRPS16) MANE Select ENSP00000362036.3:p.Ile77Thr
ENST00000372940.3:c.230T>C (MRPS16) ENSP00000362031.3:p.Ile77Thr
ENST00000372945.7:c.230T>C (MRPS16) ENSP00000362036.3:p.Ile77Thr
ENST00000471251.5:n.363T>C (MRPS16)
ENST00000473427.1:n.320T>C (MRPS16)
ENST00000479005.1:n.387T>C (MRPS16)
NM_016065.3:c.230T>C (MRPS16) NP_057149.1:p.Ile77Thr
NR_038373.1:n.175+3357A>G (DNAJC9-AS1)
XR_946059.1:n.120+66A>G
NM_016065.4:c.230T>C (MRPS16) MANE Select NP_057149.1:p.Ile77Thr