Canonical Allele Identifier: CA1932887783
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102901653G= , CM000672.2:g.102901653G= GRCh38
NC_000010.10:g.104661410G= , CM000672.1:g.104661410G= GRCh37
NC_000010.9:g.104651400G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.*953G= (AS3MT) MANE Select ENSP00000358896.3:n.*953G=
ENST00000299353.6:c.*2088G= (BORCS7-ASMT) ENSP00000299353.5:n.*2088G=
ENST00000369880.7:c.*953G= (AS3MT) ENSP00000358896.3:n.*953G=
ENST00000615257.1:c.*388G= (AS3MT) ENSP00000479361.1:n.*388G=
NM_020682.3:c.*953G= (AS3MT) NP_065733.2:n.*953G=
NR_037644.1:n.2486G= (BORCS7-ASMT)
XM_017017027.1:c.447-1143C= XP_016872516.1:n.447-1143C=
XR_001747577.1:n.169-1143C=
XR_001747578.1:n.345-1143C=
NM_020682.4:c.*953G= (AS3MT) MANE Select NP_065733.2:n.*953G=
NR_160733.1:n.169-1143C=