Canonical Allele Identifier: CA2673822548

Gene: MOCS2

Linked Data

• gnomAD v4: 5-53098583-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098583G>T , CM000667.2:g.53098583G>T	GRCh38
NC_000005.9:g.52394413G>T , CM000667.1:g.52394413G>T	GRCh37
NC_000005.8:g.52430170G>T	NCBI36
NG_008435.2:g.16186C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*19C>A MANE Select	ENSP00000380157.3:n.*19C>A
ENST00000450852.8:c.*506C>A MANE Plus Clinical	ENSP00000411022.3:n.*506C>A
ENST00000361377.8:c.*355C>A	ENSP00000355160.4:n.*355C>A
ENST00000396954.7:c.*19C>A	ENSP00000380157.3:n.*19C>A
ENST00000450852.7:c.*506C>A	ENSP00000411022.3:n.*506C>A
ENST00000502402.5:n.2333C>A
ENST00000508922.5:c.*426C>A	ENSP00000426274.1:n.*426C>A
ENST00000510818.6:c.*459C>A	ENSP00000424267.2:n.*459C>A
ENST00000582677.5:c.*227C>A	ENSP00000462870.1:n.*227C>A
ENST00000584946.5:c.*378C>A	ENSP00000464663.1:n.*378C>A
NM_004531.4:c.*19C>A	NP_004522.1:n.*19C>A
NM_176806.3:c.*506C>A	NP_789776.1:n.*506C>A
NM_004531.5:c.*19C>A MANE Select	NP_004522.1:n.*19C>A
NM_176806.4:c.*506C>A MANE Plus Clinical	NP_789776.1:n.*506C>A