Canonical Allele Identifier: CA400022251

Gene: MYL4

Linked Data

• dbSNP Id: rs2064857183
• MyVariant Identifiers: chr17:g.45299091C>G (hg19) ; chr17:g.47221725C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47221725C>G , CM000679.2:g.47221725C>G	GRCh38
NC_000017.10:g.45299091C>G , CM000679.1:g.45299091C>G	GRCh37
NC_000017.9:g.42654090C>G	NCBI36
NG_052847.1:g.17709C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354968.5:c.357C>G	ENSP00000347055.1:p.Ile119Met
ENST00000393450.5:c.357C>G MANE Select	ENSP00000377096.1:p.Ile119Met
ENST00000536623.6:c.357C>G	ENSP00000442375.2:p.Ile119Met
ENST00000570671.1:c.68C>G
ENST00000570772.5:c.*143C>G	ENSP00000458194.1:n.*143C>G
ENST00000571981.5:c.*143C>G	ENSP00000459035.1:n.*143C>G
ENST00000572303.1:c.450C>G	ENSP00000461747.1:p.Ile150Met
ENST00000572316.5:c.357C>G	ENSP00000461570.1:p.Ile119Met
ENST00000573747.6:c.314-7C>G	ENSP00000460734.1:n.314-7C>G
ENST00000576874.5:c.357C>G	ENSP00000458907.1:p.Ile119Met
NM_001002841.1:c.357C>G	NP_001002841.1:p.Ile119Met
NM_002476.2:c.357C>G MANE Select	NP_002467.1:p.Ile119Met
XM_005257391.3:c.357C>G	XP_005257448.1:p.Ile119Met
XM_011524838.1:c.357C>G	XP_011523140.1:p.Ile119Met
XM_011524839.1:c.147C>G	XP_011523141.1:p.Ile49Met
XM_005257391.5:c.357C>G	XP_005257448.1:p.Ile119Met
XM_011524839.2:c.450C>G	XP_011523141.2:p.Ile150Met
XM_017024683.1:c.450C>G	XP_016880172.1:p.Ile150Met
XM_024450766.1:c.450C>G	XP_024306534.1:p.Ile150Met
NM_001002841.2:c.357C>G	NP_001002841.1:p.Ile119Met