Canonical Allele Identifier: CA2303040326
Gene: MEX3C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.51192093_51192094delinsCA , CM000680.2:g.51192093_51192094delinsCA GRCh38
NC_000018.9:g.48718463_48718464delinsCA , CM000680.1:g.48718463_48718464delinsCA GRCh37
NC_000018.8:g.46972461_46972462delinsCA NCBI36
NG_015801.1:g.10588_10589delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000406189.4:c.754+4473_754+4474delinsTG MANE Select ENSP00000385610.3:n.754+4473_754+4474delinsTG
ENST00000591040.2:c.-107-14518_-107-14517delinsTG ENSP00000502049.1:n.-107-14518_-107-14517delinsTG
ENST00000406189.3:c.754+4473_754+4474delinsTG ENSP00000385610.3:n.754+4473_754+4474delinsTG
ENST00000591040.1:n.44-14518_44-14517delinsTG
ENST00000616921.1:c.244+4473_244+4474delinsTG ENSP00000482566.1:n.244+4473_244+4474delinsTG
NM_016626.4:c.754+4473_754+4474delinsTG NP_057710.3:n.754+4473_754+4474delinsTG
NM_016626.5:c.754+4473_754+4474delinsTG MANE Select NP_057710.3:n.754+4473_754+4474delinsTG