Canonical Allele Identifier: CA117952
Gene: MOCS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53109716_53109738del , CM000667.2:g.53109716_53109738del GRCh38
NC_000005.9:g.52405546_52405568del , CM000667.1:g.52405546_52405568del GRCh37
NC_000005.8:g.52441303_52441325del NCBI36
NG_008435.2:g.5032_5054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396954.8:c.-656_-634del MANE Select ENSP00000380157.3:n.-656_-634del
ENST00000450852.8:c.-8_15del
ENST00000361377.8:c.-8_15del
ENST00000396954.7:c.-656_-634del ENSP00000380157.3:n.-656_-634del
ENST00000450852.7:c.-8_15del
ENST00000508922.5:c.-8_15del
ENST00000510818.6:c.-8_15del
ENST00000527216.5:c.3+248_3+270del ENSP00000435326.1:n.3+248_3+270del
ENST00000582677.5:c.-8_15del
ENST00000584946.5:c.-8_15del
NM_004531.4:c.-656_-634del NP_004522.1:n.-656_-634del
NM_176806.3:c.-8_15del
NM_004531.5:c.-656_-634del MANE Select NP_004522.1:n.-656_-634del
NM_176806.4:c.-8_15del
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