Canonical Allele Identifier: CA807299409

Gene: MYO10

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.16913746G>T , CM000667.2:g.16913746G>T	GRCh38
NC_000005.9:g.16913855G>T , CM000667.1:g.16913855G>T	GRCh37
NC_000005.8:g.16966855G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000513610.6:c.21+22042C>A MANE Select	ENSP00000421280.1:n.21+22042C>A
ENST00000274203.13:c.21+22042C>A	ENSP00000274203.10:n.21+22042C>A
ENST00000502436.5:c.21+22042C>A	ENSP00000426783.2:n.21+22042C>A
ENST00000507288.1:c.21+22042C>A	ENSP00000426664.1:n.21+22042C>A
ENST00000513610.5:c.21+22042C>A	ENSP00000421280.1:n.21+22042C>A
ENST00000513882.5:c.54+2309C>A	ENSP00000421309.1:n.54+2309C>A
NM_012334.2:c.21+22042C>A	NP_036466.2:n.21+22042C>A
XM_006714475.1:c.21+22042C>A	XP_006714538.1:n.21+22042C>A
XM_006714475.3:c.21+22042C>A	XP_006714538.1:n.21+22042C>A
NM_012334.3:c.21+22042C>A MANE Select	NP_036466.2:n.21+22042C>A