Canonical Allele Identifier: CA1546395289
Gene: MOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.53098455C= , CM000667.2:g.53098455C= GRCh38
NC_000005.9:g.52394285C= , CM000667.1:g.52394285C= GRCh37
NC_000005.8:g.52430042C= NCBI36
NG_008435.2:g.16314G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396954.8:c.*147G= MANE Select ENSP00000380157.3:n.*147G=
ENST00000450852.8:c.*634G= MANE Plus Clinical ENSP00000411022.3:n.*634G=
ENST00000361377.8:c.*483G= ENSP00000355160.4:n.*483G=
ENST00000396954.7:c.*147G= ENSP00000380157.3:n.*147G=
ENST00000450852.7:c.*634G= ENSP00000411022.3:n.*634G=
ENST00000502402.5:n.2461G=
ENST00000508922.5:c.*554G= ENSP00000426274.1:n.*554G=
ENST00000510818.6:c.*587G= ENSP00000424267.2:n.*587G=
ENST00000582677.5:c.*355G= ENSP00000462870.1:n.*355G=
NM_004531.4:c.*147G= NP_004522.1:n.*147G=
NM_176806.3:c.*634G= NP_789776.1:n.*634G=
NM_004531.5:c.*147G= MANE Select NP_004522.1:n.*147G=
NM_176806.4:c.*634G= MANE Plus Clinical NP_789776.1:n.*634G=