Canonical Allele Identifier: CA500433896

Gene: MYL4

Linked Data

• MyVariant Identifiers: chr17:g.45299127C>G (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354968.5:c.393C>G	ENSP00000347055.1:p.Thr131=
ENST00000393450.5:c.393C>G MANE Select	ENSP00000377096.1:p.Thr131=
ENST00000536623.6:c.393C>G	ENSP00000442375.2:p.Thr131=
ENST00000570671.1:c.104C>G
ENST00000570772.5:c.*179C>G	ENSP00000458194.1:n.*179C>G
ENST00000571981.5:c.*179C>G	ENSP00000459035.1:n.*179C>G
ENST00000572303.1:c.486C>G	ENSP00000461747.1:p.Thr162=
ENST00000572316.5:c.393C>G	ENSP00000461570.1:p.Thr131=
ENST00000573747.6:c.343C>G	ENSP00000460734.1:p.Leu115Val
ENST00000576874.5:c.393C>G	ENSP00000458907.1:p.Thr131=
NM_001002841.1:c.393C>G	NP_001002841.1:p.Thr131=
NM_002476.2:c.393C>G MANE Select	NP_002467.1:p.Thr131=
XM_005257391.3:c.393C>G	XP_005257448.1:p.Thr131=
XM_011524838.1:c.393C>G	XP_011523140.1:p.Thr131=
XM_011524839.1:c.183C>G	XP_011523141.1:p.Thr61=
XM_005257391.5:c.393C>G	XP_005257448.1:p.Thr131=
XM_011524839.2:c.486C>G	XP_011523141.2:p.Thr162=
XM_017024683.1:c.486C>G	XP_016880172.1:p.Thr162=
XM_024450766.1:c.486C>G	XP_024306534.1:p.Thr162=
NM_001002841.2:c.393C>G	NP_001002841.1:p.Thr131=