Canonical Allele Identifier: CA2280863969

Gene: MYOM1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.3079169A= , CM000680.2:g.3079169A=	GRCh38
NC_000018.9:g.3079167A= , CM000680.1:g.3079167A=	GRCh37
NC_000018.8:g.3069167A=	NCBI36
NG_032120.1:g.145940T= , LRG_426:g.145940T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356443.9:c.4648+10T= MANE Select	ENSP00000348821.4:n.4648+10T=
ENST00000261606.11:c.4360+10T=	ENSP00000261606.7:n.4360+10T=
ENST00000356443.8:c.4648+10T=	ENSP00000348821.4:n.4648+10T=
ENST00000400569.7:c.3949+10T=	ENSP00000383413.4:n.3949+10T=
ENST00000581075.1:c.660+10T=	ENSP00000462039.1:n.660+10T=
NM_003803.3:c.4648+10T= , LRG_426t1:c.4648+10T=	NP_003794.3:n.4648+10T=
NM_019856.1:c.4360+10T=	NP_062830.1:n.4360+10T=
XM_017026062.1:c.4612+10T=	XP_016881551.1:n.4612+10T=
XM_024451281.1:c.4747+10T=	XP_024307049.1:n.4747+10T=
NM_003803.4:c.4648+10T= MANE Select	NP_003794.3:n.4648+10T=
NM_019856.2:c.4360+10T=	NP_062830.1:n.4360+10T=