Canonical Allele Identifier: CA400022322

Gene: MYL4

Linked Data

• MyVariant Identifiers: chr17:g.45299123G>T (hg19) ; chr17:g.47221757G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47221757G>T , CM000679.2:g.47221757G>T	GRCh38
NC_000017.10:g.45299123G>T , CM000679.1:g.45299123G>T	GRCh37
NC_000017.9:g.42654122G>T	NCBI36
NG_052847.1:g.17741G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354968.5:c.389G>T	ENSP00000347055.1:p.Gly130Val
ENST00000393450.5:c.389G>T MANE Select	ENSP00000377096.1:p.Gly130Val
ENST00000536623.6:c.389G>T	ENSP00000442375.2:p.Gly130Val
ENST00000570671.1:c.100G>T
ENST00000570772.5:c.*175G>T	ENSP00000458194.1:n.*175G>T
ENST00000571981.5:c.*175G>T	ENSP00000459035.1:n.*175G>T
ENST00000572303.1:c.482G>T	ENSP00000461747.1:p.Gly161Val
ENST00000572316.5:c.389G>T	ENSP00000461570.1:p.Gly130Val
ENST00000573747.6:c.339G>T	ENSP00000460734.1:p.Gly113=
ENST00000576874.5:c.389G>T	ENSP00000458907.1:p.Gly130Val
NM_001002841.1:c.389G>T	NP_001002841.1:p.Gly130Val
NM_002476.2:c.389G>T MANE Select	NP_002467.1:p.Gly130Val
XM_005257391.3:c.389G>T	XP_005257448.1:p.Gly130Val
XM_011524838.1:c.389G>T	XP_011523140.1:p.Gly130Val
XM_011524839.1:c.179G>T	XP_011523141.1:p.Gly60Val
XM_005257391.5:c.389G>T	XP_005257448.1:p.Gly130Val
XM_011524839.2:c.482G>T	XP_011523141.2:p.Gly161Val
XM_017024683.1:c.482G>T	XP_016880172.1:p.Gly161Val
XM_024450766.1:c.482G>T	XP_024306534.1:p.Gly161Val
NM_001002841.2:c.389G>T	NP_001002841.1:p.Gly130Val