Canonical Allele Identifier: CA1526954981
Gene: CMBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286357_10286361delinsAGACG , CM000667.2:g.10286357_10286361delinsAGACG GRCh38
NC_000005.9:g.10286469_10286473delinsAGACG , CM000667.1:g.10286469_10286473delinsAGACG GRCh37
NC_000005.8:g.10339469_10339473delinsAGACG NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296658.4:c.459_463delinsCGTCT MANE Select ENSP00000296658.3:p.Ser153=
ENST00000296658.3:c.459_463delinsCGTCT ENSP00000296658.3:p.Ser153=
ENST00000506821.1:n.713_717delinsCGTCT
ENST00000510532.5:n.527_531delinsCGTCT
ENST00000511963.5:n.567_571delinsCGTCT
NM_138809.3:c.459_463delinsCGTCT NP_620164.1:p.Ser153=
NM_138809.4:c.459_463delinsCGTCT MANE Select NP_620164.1:p.Ser153=