Canonical Allele Identifier: CA1932887782
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102901649A= , CM000672.2:g.102901649A= GRCh38
NC_000010.10:g.104661406A= , CM000672.1:g.104661406A= GRCh37
NC_000010.9:g.104651396A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000369880.8:c.*949A= (AS3MT) MANE Select ENSP00000358896.3:n.*949A=
ENST00000299353.6:c.*2084A= (BORCS7-ASMT) ENSP00000299353.5:n.*2084A=
ENST00000369880.7:c.*949A= (AS3MT) ENSP00000358896.3:n.*949A=
ENST00000615257.1:c.*384A= (AS3MT) ENSP00000479361.1:n.*384A=
NM_020682.3:c.*949A= (AS3MT) NP_065733.2:n.*949A=
NR_037644.1:n.2482A= (BORCS7-ASMT)
XM_017017027.1:c.447-1139T= XP_016872516.1:n.447-1139T=
XR_001747577.1:n.169-1139T=
XR_001747578.1:n.345-1139T=
NM_020682.4:c.*949A= (AS3MT) MANE Select NP_065733.2:n.*949A=
NR_160733.1:n.169-1139T=