Canonical Allele Identifier: CA493770002

Gene: MYH11 NDE1

Linked Data

• gnomAD v4: 16-15732520-A-G
• MyVariant Identifiers: chr16:g.15826377A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.15732520A>G , CM000678.2:g.15732520A>G	GRCh38
NC_000016.9:g.15826377A>G , CM000678.1:g.15826377A>G	GRCh37
NC_000016.8:g.15733878A>G	NCBI36
NG_009299.1:g.129511T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000300036.6:c.3651+44T>C (MYH11) MANE Select	ENSP00000300036.5:n.3651+44T>C
ENST00000452625.7:c.3672+44T>C (MYH11) MANE Plus Clinical	ENSP00000407821.2:n.3672+44T>C
ENST00000576790.7:c.3651+44T>C (MYH11)	ENSP00000458731.1:n.3651+44T>C
ENST00000652121.1:c.*1834+44T>C (MYH11)	ENSP00000498314.1:n.*1834+44T>C
ENST00000674538.1:c.*1404A>G (NDE1)	ENSP00000501547.1:n.*1404A>G
ENST00000674554.1:c.*904A>G (NDE1)	ENSP00000502635.1:n.*904A>G
ENST00000674588.1:c.*2603A>G (NDE1)	ENSP00000502802.1:n.*2603A>G
ENST00000674888.1:c.*904A>G (NDE1)	ENSP00000501936.1:n.*904A>G
ENST00000674900.1:c.*1313A>G (NDE1)	ENSP00000502662.1:n.*1313A>G
ENST00000674995.1:c.*2603A>G (NDE1)	ENSP00000502414.1:n.*2603A>G
ENST00000675171.1:c.*1664A>G (NDE1)	ENSP00000501812.1:n.*1664A>G
ENST00000675926.1:c.*904A>G (NDE1)	ENSP00000502354.1:n.*904A>G
ENST00000675951.1:c.*2785A>G (NDE1)	ENSP00000502160.1:n.*2785A>G
ENST00000300036.5:c.3651+44T>C (MYH11)	ENSP00000300036.5:n.3651+44T>C
ENST00000396324.7:c.3672+44T>C (MYH11)	ENSP00000379616.3:n.3672+44T>C
ENST00000452625.6:c.3672+44T>C (MYH11)	ENSP00000407821.2:n.3672+44T>C
ENST00000576790.6:c.3651+44T>C (MYH11)	ENSP00000458731.1:n.3651+44T>C
ENST00000616439.4:c.3672+44T>C (MYH11)	ENSP00000484924.1:n.3672+44T>C
NM_001040113.1:c.3672+44T>C (MYH11)	NP_001035202.1:n.3672+44T>C
NM_001040114.1:c.3672+44T>C (MYH11)	NP_001035203.1:n.3672+44T>C
NM_002474.2:c.3651+44T>C (MYH11)	NP_002465.1:n.3651+44T>C
NM_022844.2:c.3651+44T>C (MYH11)	NP_074035.1:n.3651+44T>C
XM_011522502.1:c.3651+44T>C (MYH11)	XP_011520804.1:n.3651+44T>C
XM_011522502.2:c.3651+44T>C (MYH11)	XP_011520804.1:n.3651+44T>C
XM_017023250.1:c.3672+44T>C (MYH11)	XP_016878739.1:n.3672+44T>C
NM_002474.3:c.3651+44T>C (MYH11) MANE Select	NP_002465.1:n.3651+44T>C
NM_001040113.2:c.3672+44T>C (MYH11) MANE Plus Clinical	NP_001035202.1:n.3672+44T>C
NM_001040114.2:c.3672+44T>C (MYH11)	NP_001035203.1:n.3672+44T>C
NM_022844.3:c.3651+44T>C (MYH11)	NP_074035.1:n.3651+44T>C