Canonical Allele Identifier: CA1267977629
Gene: SMYD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88082217T= , CM000664.2:g.88082217T= GRCh38
NC_000002.11:g.88381736T= , CM000664.1:g.88381736T= GRCh37
NC_000002.10:g.88162851T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000419482.7:c.138-2099T= MANE Select ENSP00000393453.2:n.138-2099T=
ENST00000419482.6:c.138-2099T= ENSP00000393453.2:n.138-2099T=
ENST00000438570.1:c.138-2099T= ENSP00000387482.1:n.138-2099T=
ENST00000444564.2:c.138-2099T= ENSP00000407888.2:n.138-2099T=
NM_198274.3:c.138-2099T= NP_938015.1:n.138-2099T=
XM_005264156.2:c.138-2099T= XP_005264213.1:n.138-2099T=
NM_001330364.1:c.138-2099T= NP_001317293.1:n.138-2099T=
NM_198274.4:c.138-2099T= MANE Select NP_938015.1:n.138-2099T=
NM_001330364.2:c.138-2099T= NP_001317293.1:n.138-2099T=