Canonical Allele Identifier: CA500433899
Gene: MYL4 HGNC NCBI

Linked Data

dbSNP Id: rs1271247073

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.47221761C>A , CM000679.2:g.47221761C>A GRCh38
NC_000017.10:g.45299127C>A , CM000679.1:g.45299127C>A GRCh37
NC_000017.9:g.42654126C>A NCBI36
NG_052847.1:g.17745C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000354968.5:c.393C>A ENSP00000347055.1:p.Thr131=
ENST00000393450.5:c.393C>A MANE Select ENSP00000377096.1:p.Thr131=
ENST00000536623.6:c.393C>A ENSP00000442375.2:p.Thr131=
ENST00000570671.1:c.104C>A
ENST00000570772.5:c.*179C>A ENSP00000458194.1:n.*179C>A
ENST00000571981.5:c.*179C>A ENSP00000459035.1:n.*179C>A
ENST00000572303.1:c.486C>A ENSP00000461747.1:p.Thr162=
ENST00000572316.5:c.393C>A ENSP00000461570.1:p.Thr131=
ENST00000573747.6:c.343C>A ENSP00000460734.1:p.Leu115Ile
ENST00000576874.5:c.393C>A ENSP00000458907.1:p.Thr131=
NM_001002841.1:c.393C>A NP_001002841.1:p.Thr131=
NM_002476.2:c.393C>A MANE Select NP_002467.1:p.Thr131=
XM_005257391.3:c.393C>A XP_005257448.1:p.Thr131=
XM_011524838.1:c.393C>A XP_011523140.1:p.Thr131=
XM_011524839.1:c.183C>A XP_011523141.1:p.Thr61=
XM_005257391.5:c.393C>A XP_005257448.1:p.Thr131=
XM_011524839.2:c.486C>A XP_011523141.2:p.Thr162=
XM_017024683.1:c.486C>A XP_016880172.1:p.Thr162=
XM_024450766.1:c.486C>A XP_024306534.1:p.Thr162=
NM_001002841.2:c.393C>A NP_001002841.1:p.Thr131=