Canonical Allele Identifier: CA8267514

Gene: MYO1C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1477882A>C , CM000679.2:g.1477882A>C	GRCh38
NC_000017.10:g.1381176A>C , CM000679.1:g.1381176A>C	GRCh37
NC_000017.9:g.1327926A>C	NCBI36
NG_047063.1:g.19826T>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001080779.2:c.1482+9T>G MANE Select	NP_001074248.1:n.1482+9T>G
ENST00000648651.1:c.1482+9T>G MANE Select	ENSP00000496954.1:n.1482+9T>G
NM_001080779.1:c.1482+9T>G	NP_001074248.1:n.1482+9T>G
NM_001080950.1:c.1425+9T>G	NP_001074419.1:n.1425+9T>G
NM_001080950.2:c.1425+9T>G	NP_001074419.1:n.1425+9T>G
NM_001363855.1:c.1410+9T>G	NP_001350784.1:n.1410+9T>G
NM_033375.4:c.1377+9T>G	NP_203693.3:n.1377+9T>G
NM_033375.5:c.1377+9T>G	NP_203693.3:n.1377+9T>G
ENST00000359786.9:c.1482+9T>G	ENSP00000352834.5:n.1482+9T>G
ENST00000361007.6:c.1377+9T>G	ENSP00000354283.2:n.1377+9T>G
ENST00000361007.7:c.1377+9T>G	ENSP00000354283.2:n.1377+9T>G
ENST00000438665.6:c.1425+9T>G	ENSP00000412197.2:n.1425+9T>G
ENST00000545534.6:c.1410+9T>G	ENSP00000437685.2:n.1410+9T>G
ENST00000570984.7:c.1377+9T>G	ENSP00000459271.3:n.1377+9T>G
ENST00000573961.1:n.136+9T>G
ENST00000575158.5:c.1377+9T>G	ENSP00000459174.1:n.1377+9T>G
ENST00000646049.1:c.1377+9T>G	ENSP00000493973.1:n.1377+9T>G
ENST00000648446.1:c.1425+9T>G	ENSP00000496799.1:n.1425+9T>G
XM_024450768.1:c.1377+9T>G	XP_024306536.1:n.1377+9T>G
XM_024450769.1:c.1377+9T>G	XP_024306537.1:n.1377+9T>G