Canonical Allele Identifier: CA2262577760

Gene: MYL4

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.47221998T= , CM000679.2:g.47221998T=	GRCh38
NC_000017.10:g.45299364T= , CM000679.1:g.45299364T=	GRCh37
NC_000017.9:g.42654363T=	NCBI36
NG_052847.1:g.17982T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000354968.5:c.487+143T=	ENSP00000347055.1:n.487+143T=
ENST00000393450.5:c.487+143T= MANE Select	ENSP00000377096.1:n.487+143T=
ENST00000536623.6:c.487+143T=	ENSP00000442375.2:n.487+143T=
ENST00000570671.1:c.198+143T=
ENST00000571981.5:c.*273+143T=	ENSP00000459035.1:n.*273+143T=
ENST00000572316.5:c.487+143T=	ENSP00000461570.1:n.487+143T=
ENST00000573747.6:c.*89+143T=	ENSP00000460734.1:n.*89+143T=
ENST00000576874.5:c.487+143T=	ENSP00000458907.1:n.487+143T=
NM_001002841.1:c.487+143T=	NP_001002841.1:n.487+143T=
NM_002476.2:c.487+143T= MANE Select	NP_002467.1:n.487+143T=
XM_005257391.3:c.487+143T=	XP_005257448.1:n.487+143T=
XM_011524838.1:c.487+143T=	XP_011523140.1:n.487+143T=
XM_011524839.1:c.277+143T=	XP_011523141.1:n.277+143T=
XM_005257391.5:c.487+143T=	XP_005257448.1:n.487+143T=
XM_011524839.2:c.580+143T=	XP_011523141.2:n.580+143T=
XM_017024683.1:c.580+143T=	XP_016880172.1:n.580+143T=
XM_024450766.1:c.580+143T=	XP_024306534.1:n.580+143T=
NM_001002841.2:c.487+143T=	NP_001002841.1:n.487+143T=