Canonical Allele Identifier: CA2673822561

Gene: MOCS2

Linked Data

• gnomAD v4: 5-53098673-A-AGT

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098673_53098674insGT , CM000667.2:g.53098673_53098674insGT	GRCh38
NC_000005.9:g.52394503_52394504insGT , CM000667.1:g.52394503_52394504insGT	GRCh37
NC_000005.8:g.52430260_52430261insGT	NCBI36
NG_008435.2:g.16095_16096insAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.502-7_502-6insAC MANE Select	ENSP00000380157.3:n.502-7_502-6insAC
ENST00000450852.8:c.*422-7_*422-6insAC MANE Plus Clinical	ENSP00000411022.3:n.*422-7_*422-6insAC
ENST00000361377.8:c.*271-7_*271-6insAC	ENSP00000355160.4:n.*271-7_*271-6insAC
ENST00000396954.7:c.502-7_502-6insAC	ENSP00000380157.3:n.502-7_502-6insAC
ENST00000450852.7:c.*422-7_*422-6insAC	ENSP00000411022.3:n.*422-7_*422-6insAC
ENST00000502402.5:n.2249-7_2249-6insAC
ENST00000508922.5:c.*335_*336insAC	ENSP00000426274.1:n.*335_*336insAC
ENST00000510818.6:c.*375-7_*375-6insAC	ENSP00000424267.2:n.*375-7_*375-6insAC
ENST00000582677.5:c.*143-7_*143-6insAC	ENSP00000462870.1:n.*143-7_*143-6insAC
ENST00000584946.5:c.*294-7_*294-6insAC	ENSP00000464663.1:n.*294-7_*294-6insAC
NM_004531.4:c.502-7_502-6insAC	NP_004522.1:n.502-7_502-6insAC
NM_176806.3:c.*422-7_*422-6insAC	NP_789776.1:n.*422-7_*422-6insAC
NM_004531.5:c.502-7_502-6insAC MANE Select	NP_004522.1:n.502-7_502-6insAC
NM_176806.4:c.*422-7_*422-6insAC MANE Plus Clinical	NP_789776.1:n.*422-7_*422-6insAC