Canonical Allele Identifier: CA137074

Gene: MYO3A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26166161G>A , CM000672.2:g.26166161G>A	GRCh38
NC_000010.10:g.26455090G>A , CM000672.1:g.26455090G>A	GRCh37
NC_000010.9:g.26495096G>A	NCBI36
NG_011635.1:g.237089G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000477691.2:n.320G>A
ENST00000642197.1:n.3298G>A
ENST00000642920.2:c.3094G>A MANE Select	ENSP00000495965.1:p.Ala1032Thr
ENST00000647478.1:c.*1089G>A	ENSP00000493932.1:n.*1089G>A
ENST00000265944.9:c.3094G>A	ENSP00000265944.4:p.Ala1032Thr
ENST00000477691.1:n.320G>A
ENST00000543632.5:c.1777-45682G>A	ENSP00000445909.1:n.1777-45682G>A
NM_017433.4:c.3094G>A	NP_059129.3:p.Ala1032Thr
XM_011519498.1:c.3094G>A	XP_011517800.1:p.Ala1032Thr
XM_011519499.1:c.3094G>A	XP_011517801.1:p.Ala1032Thr
XM_011519500.1:c.3094G>A	XP_011517802.1:p.Ala1032Thr
XM_011519501.1:c.3094G>A	XP_011517803.1:p.Ala1032Thr
XM_011519502.1:c.3094G>A	XP_011517804.1:p.Ala1032Thr
XM_011519503.1:c.3094G>A	XP_011517805.1:p.Ala1032Thr
XM_011519504.1:c.3094G>A	XP_011517806.1:p.Ala1032Thr
XM_011519505.1:c.3094G>A	XP_011517807.1:p.Ala1032Thr
XM_011519506.1:c.3094G>A	XP_011517808.1:p.Ala1032Thr
XM_011519507.1:c.2731G>A	XP_011517809.1:p.Ala911Thr
XM_011519508.1:c.3094G>A	XP_011517810.1:p.Ala1032Thr
XM_011519509.1:c.3094G>A	XP_011517811.1:p.Ala1032Thr
XM_011519510.1:c.3094G>A	XP_011517812.1:p.Ala1032Thr
XM_011519512.1:c.1222G>A	XP_011517814.1:p.Ala408Thr
XM_011519513.1:c.763G>A	XP_011517815.1:p.Ala255Thr
XR_930492.1:n.3298G>A
XR_930493.1:n.3298G>A
XR_930494.1:n.3298G>A
XR_930760.1:n.178+2320C>T
XM_011519498.2:c.3094G>A	XP_011517800.1:p.Ala1032Thr
XM_011519500.2:c.3094G>A	XP_011517802.1:p.Ala1032Thr
XM_011519506.2:c.3094G>A	XP_011517808.1:p.Ala1032Thr
XM_011519508.2:c.3094G>A	XP_011517810.1:p.Ala1032Thr
XM_011519510.2:c.3094G>A	XP_011517812.1:p.Ala1032Thr
XM_011519513.2:c.763G>A	XP_011517815.1:p.Ala255Thr
XR_001747111.1:n.3298G>A
NM_017433.5:c.3094G>A MANE Select	NP_059129.3:p.Ala1032Thr