Canonical Allele Identifier: CA2673822534

Gene: MOCS2

Linked Data

• gnomAD v4: 5-53098549-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.53098549C>A , CM000667.2:g.53098549C>A	GRCh38
NC_000005.9:g.52394379C>A , CM000667.1:g.52394379C>A	GRCh37
NC_000005.8:g.52430136C>A	NCBI36
NG_008435.2:g.16220G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000396954.8:c.*53G>T MANE Select	ENSP00000380157.3:n.*53G>T
ENST00000450852.8:c.*540G>T MANE Plus Clinical	ENSP00000411022.3:n.*540G>T
ENST00000361377.8:c.*389G>T	ENSP00000355160.4:n.*389G>T
ENST00000396954.7:c.*53G>T	ENSP00000380157.3:n.*53G>T
ENST00000450852.7:c.*540G>T	ENSP00000411022.3:n.*540G>T
ENST00000502402.5:n.2367G>T
ENST00000508922.5:c.*460G>T	ENSP00000426274.1:n.*460G>T
ENST00000510818.6:c.*493G>T	ENSP00000424267.2:n.*493G>T
ENST00000582677.5:c.*261G>T	ENSP00000462870.1:n.*261G>T
ENST00000584946.5:c.*412G>T	ENSP00000464663.1:n.*412G>T
NM_004531.4:c.*53G>T	NP_004522.1:n.*53G>T
NM_176806.3:c.*540G>T	NP_789776.1:n.*540G>T
NM_004531.5:c.*53G>T MANE Select	NP_004522.1:n.*53G>T
NM_176806.4:c.*540G>T MANE Plus Clinical	NP_789776.1:n.*540G>T