Canonical Allele Identifier: CA2673822564

Gene: MOCS2

Linked Data

• gnomAD v4: 5-53098681-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098681_53098682insGG , CM000667.2:g.53098681_53098682insGG	GRCh38
NC_000005.9:g.52394511_52394512insGG , CM000667.1:g.52394511_52394512insGG	GRCh37
NC_000005.8:g.52430268_52430269insGG	NCBI36
NG_008435.2:g.16087_16088insCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.502-15_502-14insCC MANE Select	ENSP00000380157.3:n.502-15_502-14insCC
ENST00000450852.8:c.*422-15_*422-14insCC MANE Plus Clinical	ENSP00000411022.3:n.*422-15_*422-14insCC
ENST00000361377.8:c.*271-15_*271-14insCC	ENSP00000355160.4:n.*271-15_*271-14insCC
ENST00000396954.7:c.502-15_502-14insCC	ENSP00000380157.3:n.502-15_502-14insCC
ENST00000450852.7:c.*422-15_*422-14insCC	ENSP00000411022.3:n.*422-15_*422-14insCC
ENST00000502402.5:n.2249-15_2249-14insCC
ENST00000508922.5:c.*327_*328insCC	ENSP00000426274.1:n.*327_*328insCC
ENST00000510818.6:c.*375-15_*375-14insCC	ENSP00000424267.2:n.*375-15_*375-14insCC
ENST00000582677.5:c.*143-15_*143-14insCC	ENSP00000462870.1:n.*143-15_*143-14insCC
ENST00000584946.5:c.*294-15_*294-14insCC	ENSP00000464663.1:n.*294-15_*294-14insCC
NM_004531.4:c.502-15_502-14insCC	NP_004522.1:n.502-15_502-14insCC
NM_176806.3:c.*422-15_*422-14insCC	NP_789776.1:n.*422-15_*422-14insCC
NM_004531.5:c.502-15_502-14insCC MANE Select	NP_004522.1:n.502-15_502-14insCC
NM_176806.4:c.*422-15_*422-14insCC MANE Plus Clinical	NP_789776.1:n.*422-15_*422-14insCC