Canonical Allele Identifier: CA1897925681

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212362_26212363delinsTA , CM000672.2:g.26212362_26212363delinsTA	GRCh38
NC_000010.10:g.26501291_26501292delinsTA , CM000672.1:g.26501291_26501292delinsTA	GRCh37
NC_000010.9:g.26541297_26541298delinsTA	NCBI36
NG_011635.1:g.283290_283291delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*399_*400delinsTA MANE Select	ENSP00000495965.1:n.*399_*400delinsTA
ENST00000645292.1:n.710_711delinsTA
ENST00000265944.9:c.*399_*400delinsTA	ENSP00000265944.4:n.*399_*400delinsTA
NM_017433.4:c.*399_*400delinsTA	NP_059129.3:n.*399_*400delinsTA
XM_011519498.1:c.*399_*400delinsTA	XP_011517800.1:n.*399_*400delinsTA
XM_011519499.1:c.*399_*400delinsTA	XP_011517801.1:n.*399_*400delinsTA
XM_011519500.1:c.*399_*400delinsTA	XP_011517802.1:n.*399_*400delinsTA
XM_011519501.1:c.*399_*400delinsTA	XP_011517803.1:n.*399_*400delinsTA
XM_011519504.1:c.*301_*302delinsTA	XP_011517806.1:n.*301_*302delinsTA
XM_011519505.1:c.*399_*400delinsTA	XP_011517807.1:n.*399_*400delinsTA
XM_011519507.1:c.*399_*400delinsTA	XP_011517809.1:n.*399_*400delinsTA
XM_011519512.1:c.*399_*400delinsTA	XP_011517814.1:n.*399_*400delinsTA
XM_011519513.1:c.*399_*400delinsTA	XP_011517815.1:n.*399_*400delinsTA
XR_930493.1:n.5347_5348delinsTA
XM_011519498.2:c.*399_*400delinsTA	XP_011517800.1:n.*399_*400delinsTA
XM_011519500.2:c.*399_*400delinsTA	XP_011517802.1:n.*399_*400delinsTA
XM_011519513.2:c.*399_*400delinsTA	XP_011517815.1:n.*399_*400delinsTA
XR_001747111.1:n.4307_4308delinsTA
NM_017433.5:c.*399_*400delinsTA MANE Select	NP_059129.3:n.*399_*400delinsTA