Canonical Allele Identifier: CA497280308

Gene: MYO1C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1470214C>T , CM000679.2:g.1470214C>T	GRCh38
NC_000017.10:g.1373508C>T , CM000679.1:g.1373508C>T	GRCh37
NC_000017.9:g.1320258C>T	NCBI36
NG_047063.1:g.27494G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361007.7:c.2382G>A	ENSP00000354283.2:p.Leu794=
ENST00000570984.7:c.2382G>A	ENSP00000459271.3:p.Leu794=
ENST00000646049.1:c.2382G>A	ENSP00000493973.1:p.Leu794=
ENST00000648446.1:c.2430G>A	ENSP00000496799.1:p.Leu810=
ENST00000648651.1:c.2487G>A MANE Select	ENSP00000496954.1:p.Leu829=
ENST00000359786.9:c.2487G>A	ENSP00000352834.5:p.Leu829=
ENST00000361007.6:c.2382G>A	ENSP00000354283.2:p.Leu794=
ENST00000438665.6:c.2430G>A	ENSP00000412197.2:p.Leu810=
ENST00000545534.6:c.2415G>A	ENSP00000437685.2:p.Leu805=
ENST00000572615.1:n.171G>A
ENST00000574308.1:n.6G>A
ENST00000575158.5:c.2382G>A	ENSP00000459174.1:p.Leu794=
NM_001080779.1:c.2487G>A	NP_001074248.1:p.Leu829=
NM_001080950.1:c.2430G>A	NP_001074419.1:p.Leu810=
NM_033375.4:c.2382G>A	NP_203693.3:p.Leu794=
NM_001363855.1:c.2415G>A	NP_001350784.1:p.Leu805=
XM_024450768.1:c.2382G>A	XP_024306536.1:p.Leu794=
XM_024450769.1:c.2382G>A	XP_024306537.1:p.Leu794=
NM_001080779.2:c.2487G>A MANE Select	NP_001074248.1:p.Leu829=
NM_001080950.2:c.2430G>A	NP_001074419.1:p.Leu810=
NM_033375.5:c.2382G>A	NP_203693.3:p.Leu794=