Canonical Allele Identifier: CA1932887229
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102900298G= , CM000672.2:g.102900298G= GRCh38
NC_000010.10:g.104660055G= , CM000672.1:g.104660055G= GRCh37
NC_000010.9:g.104650045G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.1021-295G= (AS3MT) MANE Select ENSP00000358896.3:n.1021-295G=
ENST00000299353.6:c.*1028-295G= (BORCS7-ASMT) ENSP00000299353.5:n.*1028-295G=
ENST00000369880.7:c.1021-295G= (AS3MT) ENSP00000358896.3:n.1021-295G=
ENST00000615257.1:c.*3-295G= (AS3MT) ENSP00000479361.1:n.*3-295G=
NM_020682.3:c.1021-295G= (AS3MT) NP_065733.2:n.1021-295G=
NR_037644.1:n.1426-295G= (BORCS7-ASMT)
XM_017017027.1:c.*92+96C= XP_016872516.1:n.*92+96C=
XR_001747577.1:n.285+96C=
XR_001747578.1:n.461+96C=
NM_020682.4:c.1021-295G= (AS3MT) MANE Select NP_065733.2:n.1021-295G=
NR_160733.1:n.285+96C=