Canonical Allele Identifier: CA1932887211

Gene: AS3MT BORCS7-ASMT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.102900267T= , CM000672.2:g.102900267T=	GRCh38
NC_000010.10:g.104660024T= , CM000672.1:g.104660024T=	GRCh37
NC_000010.9:g.104650014T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000369880.8:c.1021-326T= (AS3MT) MANE Select	ENSP00000358896.3:n.1021-326T=
ENST00000299353.6:c.*1028-326T= (BORCS7-ASMT)	ENSP00000299353.5:n.*1028-326T=
ENST00000369880.7:c.1021-326T= (AS3MT)	ENSP00000358896.3:n.1021-326T=
ENST00000615257.1:c.*3-326T= (AS3MT)	ENSP00000479361.1:n.*3-326T=
NM_020682.3:c.1021-326T= (AS3MT)	NP_065733.2:n.1021-326T=
NR_037644.1:n.1426-326T= (BORCS7-ASMT)
XM_017017027.1:c.*92+127A=	XP_016872516.1:n.*92+127A=
XR_001747577.1:n.285+127A=
XR_001747578.1:n.461+127A=
NM_020682.4:c.1021-326T= (AS3MT) MANE Select	NP_065733.2:n.1021-326T=
NR_160733.1:n.285+127A=