Canonical Allele Identifier: CA663259925

Gene: MYO3A

Linked Data

• dbSNP Id: rs1236863320
• gnomAD v3: 10-26212242-T-C
• gnomAD v4: 10-26212242-T-C
• MyVariant Identifiers: chr10:g.26501171T>C (hg19) ; chr10:g.26212242T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.26212242T>C , CM000672.2:g.26212242T>C	GRCh38
NC_000010.10:g.26501171T>C , CM000672.1:g.26501171T>C	GRCh37
NC_000010.9:g.26541177T>C	NCBI36
NG_011635.1:g.283170T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642920.2:c.*279T>C MANE Select	ENSP00000495965.1:n.*279T>C
ENST00000644253.1:n.796T>C
ENST00000645292.1:n.590T>C
ENST00000265944.9:c.*279T>C	ENSP00000265944.4:n.*279T>C
NM_017433.4:c.*279T>C	NP_059129.3:n.*279T>C
XM_011519498.1:c.*279T>C	XP_011517800.1:n.*279T>C
XM_011519499.1:c.*279T>C	XP_011517801.1:n.*279T>C
XM_011519500.1:c.*279T>C	XP_011517802.1:n.*279T>C
XM_011519501.1:c.*279T>C	XP_011517803.1:n.*279T>C
XM_011519504.1:c.*181T>C	XP_011517806.1:n.*181T>C
XM_011519505.1:c.*279T>C	XP_011517807.1:n.*279T>C
XM_011519507.1:c.*279T>C	XP_011517809.1:n.*279T>C
XM_011519512.1:c.*279T>C	XP_011517814.1:n.*279T>C
XM_011519513.1:c.*279T>C	XP_011517815.1:n.*279T>C
XR_930493.1:n.5227T>C
XM_011519498.2:c.*279T>C	XP_011517800.1:n.*279T>C
XM_011519500.2:c.*279T>C	XP_011517802.1:n.*279T>C
XM_011519513.2:c.*279T>C	XP_011517815.1:n.*279T>C
XR_001747111.1:n.4187T>C
NM_017433.5:c.*279T>C MANE Select	NP_059129.3:n.*279T>C