Canonical Allele Identifier: CA1546395405

Gene: MOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098694_53098695delinsTA , CM000667.2:g.53098694_53098695delinsTA	GRCh38
NC_000005.9:g.52394524_52394525delinsTA , CM000667.1:g.52394524_52394525delinsTA	GRCh37
NC_000005.8:g.52430281_52430282delinsTA	NCBI36
NG_008435.2:g.16074_16075delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000396954.8:c.502-28_502-27delinsTA MANE Select	ENSP00000380157.3:n.502-28_502-27delinsTA
ENST00000450852.8:c.*422-28_*422-27delinsTA MANE Plus Clinical	ENSP00000411022.3:n.*422-28_*422-27delinsTA
ENST00000361377.8:c.*271-28_*271-27delinsTA	ENSP00000355160.4:n.*271-28_*271-27delinsTA
ENST00000396954.7:c.502-28_502-27delinsTA	ENSP00000380157.3:n.502-28_502-27delinsTA
ENST00000450852.7:c.*422-28_*422-27delinsTA	ENSP00000411022.3:n.*422-28_*422-27delinsTA
ENST00000502402.5:n.2249-28_2249-27delinsTA
ENST00000508922.5:c.*314_*315delinsTA	ENSP00000426274.1:n.*314_*315delinsTA
ENST00000510818.6:c.*375-28_*375-27delinsTA	ENSP00000424267.2:n.*375-28_*375-27delinsTA
ENST00000582677.5:c.*143-28_*143-27delinsTA	ENSP00000462870.1:n.*143-28_*143-27delinsTA
ENST00000584946.5:c.*294-28_*294-27delinsTA	ENSP00000464663.1:n.*294-28_*294-27delinsTA
NM_004531.4:c.502-28_502-27delinsTA	NP_004522.1:n.502-28_502-27delinsTA
NM_176806.3:c.*422-28_*422-27delinsTA	NP_789776.1:n.*422-28_*422-27delinsTA
NM_004531.5:c.502-28_502-27delinsTA MANE Select	NP_004522.1:n.502-28_502-27delinsTA
NM_176806.4:c.*422-28_*422-27delinsTA MANE Plus Clinical	NP_789776.1:n.*422-28_*422-27delinsTA