Canonical Allele Identifier: CA2248289428

Gene: MYOCD

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.12734054T= , CM000679.2:g.12734054T=	GRCh38
NC_000017.10:g.12637371T= , CM000679.1:g.12637371T=	GRCh37
NC_000017.9:g.12578096T=	NCBI36
NG_012972.1:g.73165T=

Transcript Alleles

HGVS	Amino-acid Change
NM_001146312.3:c.416-2107T= MANE Select	NP_001139784.1:n.416-2107T=
ENST00000425538.6:c.416-2107T= MANE Select	ENSP00000401678.1:n.416-2107T=
NM_001146312.2:c.416-2107T=	NP_001139784.1:n.416-2107T=
NM_001378306.1:c.179-2107T=	NP_001365235.1:n.179-2107T=
NM_153604.3:c.416-2107T=	NP_705832.1:n.416-2107T=
NM_153604.4:c.416-2107T=	NP_705832.1:n.416-2107T=
ENST00000343344.8:c.416-2107T=	ENSP00000341835.4:n.416-2107T=
ENST00000395988.1:n.336-2107T=
ENST00000425538.5:c.416-2107T=	ENSP00000401678.1:n.416-2107T=
XM_005256863.1:c.416-2107T=	XP_005256920.1:n.416-2107T=
XM_005256864.1:c.179-2107T=	XP_005256921.1:n.179-2107T=
XM_017025342.1:c.416-2107T=	XP_016880831.1:n.416-2107T=