Canonical Allele Identifier: CA497275525

Gene: MYO1C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1474790G>C , CM000679.2:g.1474790G>C	GRCh38
NC_000017.10:g.1378084G>C , CM000679.1:g.1378084G>C	GRCh37
NC_000017.9:g.1324834G>C	NCBI36
NG_047063.1:g.22918C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361007.7:c.1611+22C>G	ENSP00000354283.2:n.1611+22C>G
ENST00000570984.7:c.1611+22C>G	ENSP00000459271.3:n.1611+22C>G
ENST00000646049.1:c.1611+22C>G	ENSP00000493973.1:n.1611+22C>G
ENST00000648446.1:c.1659+22C>G	ENSP00000496799.1:n.1659+22C>G
ENST00000648651.1:c.1716+22C>G MANE Select	ENSP00000496954.1:n.1716+22C>G
ENST00000359786.9:c.1716+22C>G	ENSP00000352834.5:n.1716+22C>G
ENST00000361007.6:c.1611+22C>G	ENSP00000354283.2:n.1611+22C>G
ENST00000438665.6:c.1659+22C>G	ENSP00000412197.2:n.1659+22C>G
ENST00000545534.6:c.1644+22C>G	ENSP00000437685.2:n.1644+22C>G
ENST00000571615.1:n.120+22C>G
ENST00000575158.5:c.1611+22C>G	ENSP00000459174.1:n.1611+22C>G
NM_001080779.1:c.1716+22C>G	NP_001074248.1:n.1716+22C>G
NM_001080950.1:c.1659+22C>G	NP_001074419.1:n.1659+22C>G
NM_033375.4:c.1611+22C>G	NP_203693.3:n.1611+22C>G
NM_001363855.1:c.1644+22C>G	NP_001350784.1:n.1644+22C>G
XM_024450768.1:c.1611+22C>G	XP_024306536.1:n.1611+22C>G
XM_024450769.1:c.1611+22C>G	XP_024306537.1:n.1611+22C>G
NM_001080779.2:c.1716+22C>G MANE Select	NP_001074248.1:n.1716+22C>G
NM_001080950.2:c.1659+22C>G	NP_001074419.1:n.1659+22C>G
NM_033375.5:c.1611+22C>G	NP_203693.3:n.1611+22C>G