Canonical Allele Identifier: CA1932887283
Gene: AS3MT HGNC NCBI
BORCS7-ASMT HGNC NCBI

Linked Data

dbSNP Id: rs1845252148

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.102900439_102900440del , CM000672.2:g.102900439_102900440del GRCh38
NC_000010.10:g.104660196_104660197del , CM000672.1:g.104660196_104660197del GRCh37
NC_000010.9:g.104650186_104650187del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000369880.8:c.1021-154_1021-153del (AS3MT) MANE Select ENSP00000358896.3:n.1021-154_1021-153del
ENST00000299353.6:c.*1028-154_*1028-153del (BORCS7-ASMT) ENSP00000299353.5:n.*1028-154_*1028-153de...
ENST00000369880.7:c.1021-154_1021-153del (AS3MT) ENSP00000358896.3:n.1021-154_1021-153del
ENST00000615257.1:c.*3-154_*3-153del (AS3MT) ENSP00000479361.1:n.*3-154_*3-153del
NM_020682.3:c.1021-154_1021-153del (AS3MT) NP_065733.2:n.1021-154_1021-153del
NR_037644.1:n.1426-154_1426-153del (BORCS7-ASMT)
XM_017017027.1:c.*46_*47del XP_016872516.1:n.*46_*47del
XR_001747577.1:n.239_240del
XR_001747578.1:n.415_416del
NM_020682.4:c.1021-154_1021-153del (AS3MT) MANE Select NP_065733.2:n.1021-154_1021-153del
NR_160733.1:n.239_240del