Canonical Allele Identifier: CA15911245

Gene: MYO1C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1466961T>C , CM000679.2:g.1466961T>C	GRCh38
NC_000017.10:g.1370255T>C , CM000679.1:g.1370255T>C	GRCh37
NC_000017.9:g.1317005T>C	NCBI36
NG_047063.1:g.30747A>G

Transcript Alleles

HGVS	Amino-acid Change
NM_001080779.2:c.3165+281A>G MANE Select	NP_001074248.1:n.3165+281A>G
ENST00000648651.1:c.3165+281A>G MANE Select	ENSP00000496954.1:n.3165+281A>G
NM_001080779.1:c.3165+281A>G	NP_001074248.1:n.3165+281A>G
NM_001080950.1:c.3108+281A>G	NP_001074419.1:n.3108+281A>G
NM_001080950.2:c.3108+281A>G	NP_001074419.1:n.3108+281A>G
NM_001363855.1:c.3093+281A>G	NP_001350784.1:n.3093+281A>G
NM_033375.4:c.3060+281A>G	NP_203693.3:n.3060+281A>G
NM_033375.5:c.3060+281A>G	NP_203693.3:n.3060+281A>G
ENST00000359786.9:c.3165+281A>G	ENSP00000352834.5:n.3165+281A>G
ENST00000361007.6:c.3060+281A>G	ENSP00000354283.2:n.3060+281A>G
ENST00000361007.7:c.3060+281A>G	ENSP00000354283.2:n.3060+281A>G
ENST00000438665.6:c.3108+281A>G	ENSP00000412197.2:n.3108+281A>G
ENST00000545534.6:c.3093+281A>G	ENSP00000437685.2:n.3093+281A>G
ENST00000570984.7:c.3060+281A>G	ENSP00000459271.3:n.3060+281A>G
ENST00000575158.5:c.3060+281A>G	ENSP00000459174.1:n.3060+281A>G
ENST00000646049.1:c.3060+281A>G	ENSP00000493973.1:n.3060+281A>G
ENST00000648446.1:c.3108+281A>G	ENSP00000496799.1:n.3108+281A>G
XM_024450768.1:c.3060+281A>G	XP_024306536.1:n.3060+281A>G
XM_024450769.1:c.3060+281A>G	XP_024306537.1:n.3060+281A>G