Canonical Allele Identifier: CA2610731442
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102901647G>C , CM000672.2:g.102901647G>C GRCh38
NC_000010.10:g.104661404G>C , CM000672.1:g.104661404G>C GRCh37
NC_000010.9:g.104651394G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.*947G>C (AS3MT) MANE Select ENSP00000358896.3:n.*947G>C
ENST00000299353.6:c.*2082G>C (BORCS7-ASMT) ENSP00000299353.5:n.*2082G>C
ENST00000369880.7:c.*947G>C (AS3MT) ENSP00000358896.3:n.*947G>C
ENST00000615257.1:c.*382G>C (AS3MT) ENSP00000479361.1:n.*382G>C
NM_020682.3:c.*947G>C (AS3MT) NP_065733.2:n.*947G>C
NR_037644.1:n.2480G>C (BORCS7-ASMT)
XM_017017027.1:c.447-1137C>G XP_016872516.1:n.447-1137C>G
XR_001747577.1:n.169-1137C>G
XR_001747578.1:n.345-1137C>G
NM_020682.4:c.*947G>C (AS3MT) MANE Select NP_065733.2:n.*947G>C
NR_160733.1:n.169-1137C>G