Canonical Allele Identifier: CA1932887279
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102900431C= , CM000672.2:g.102900431C= GRCh38
NC_000010.10:g.104660188C= , CM000672.1:g.104660188C= GRCh37
NC_000010.9:g.104650178C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.1021-162C= (AS3MT) MANE Select ENSP00000358896.3:n.1021-162C=
ENST00000299353.6:c.*1028-162C= (BORCS7-ASMT) ENSP00000299353.5:n.*1028-162C=
ENST00000369880.7:c.1021-162C= (AS3MT) ENSP00000358896.3:n.1021-162C=
ENST00000615257.1:c.*3-162C= (AS3MT) ENSP00000479361.1:n.*3-162C=
NM_020682.3:c.1021-162C= (AS3MT) NP_065733.2:n.1021-162C=
NR_037644.1:n.1426-162C= (BORCS7-ASMT)
XM_017017027.1:c.*55G= XP_016872516.1:n.*55G=
XR_001747577.1:n.248G=
XR_001747578.1:n.424G=
NM_020682.4:c.1021-162C= (AS3MT) MANE Select NP_065733.2:n.1021-162C=
NR_160733.1:n.248G=