Canonical Allele Identifier: CA1932887788
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102901665G= , CM000672.2:g.102901665G= GRCh38
NC_000010.10:g.104661422G= , CM000672.1:g.104661422G= GRCh37
NC_000010.9:g.104651412G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.*965G= (AS3MT) MANE Select ENSP00000358896.3:n.*965G=
ENST00000299353.6:c.*2100G= (BORCS7-ASMT) ENSP00000299353.5:n.*2100G=
ENST00000369880.7:c.*965G= (AS3MT) ENSP00000358896.3:n.*965G=
ENST00000615257.1:c.*400G= (AS3MT) ENSP00000479361.1:n.*400G=
NM_020682.3:c.*965G= (AS3MT) NP_065733.2:n.*965G=
NR_037644.1:n.2498G= (BORCS7-ASMT)
XM_017017027.1:c.447-1155C= XP_016872516.1:n.447-1155C=
XR_001747577.1:n.169-1155C=
XR_001747578.1:n.345-1155C=
NM_020682.4:c.*965G= (AS3MT) MANE Select NP_065733.2:n.*965G=
NR_160733.1:n.169-1155C=