Canonical Allele Identifier: CA8267013

Gene: MYO1C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1470318C>T , CM000679.2:g.1470318C>T	GRCh38
NC_000017.10:g.1373612C>T , CM000679.1:g.1373612C>T	GRCh37
NC_000017.9:g.1320362C>T	NCBI36
NG_047063.1:g.27390G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361007.7:c.2278G>A	ENSP00000354283.2:p.Val760Ile
ENST00000570984.7:c.2278G>A	ENSP00000459271.3:p.Val760Ile
ENST00000646049.1:c.2278G>A	ENSP00000493973.1:p.Val760Ile
ENST00000648446.1:c.2326G>A	ENSP00000496799.1:p.Val776Ile
ENST00000648651.1:c.2383G>A MANE Select	ENSP00000496954.1:p.Val795Ile
ENST00000359786.9:c.2383G>A	ENSP00000352834.5:p.Val795Ile
ENST00000361007.6:c.2278G>A	ENSP00000354283.2:p.Val760Ile
ENST00000438665.6:c.2326G>A	ENSP00000412197.2:p.Val776Ile
ENST00000545534.6:c.2311G>A	ENSP00000437685.2:p.Val771Ile
ENST00000572615.1:n.67G>A
ENST00000575011.1:c.307G>A
ENST00000575158.5:c.2278G>A	ENSP00000459174.1:p.Val760Ile
NM_001080779.1:c.2383G>A	NP_001074248.1:p.Val795Ile
NM_001080950.1:c.2326G>A	NP_001074419.1:p.Val776Ile
NM_033375.4:c.2278G>A	NP_203693.3:p.Val760Ile
NM_001363855.1:c.2311G>A	NP_001350784.1:p.Val771Ile
XM_024450768.1:c.2278G>A	XP_024306536.1:p.Val760Ile
XM_024450769.1:c.2278G>A	XP_024306537.1:p.Val760Ile
NM_001080779.2:c.2383G>A MANE Select	NP_001074248.1:p.Val795Ile
NM_001080950.2:c.2326G>A	NP_001074419.1:p.Val776Ile
NM_033375.5:c.2278G>A	NP_203693.3:p.Val760Ile