Canonical Allele Identifier: CA386279231

Gene: MYBPC1

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.101636674G>C , CM000674.2:g.101636674G>C	GRCh38
NC_000012.11:g.102030452G>C , CM000674.1:g.102030452G>C	GRCh37
NC_000012.10:g.100554583G>C	NCBI36
NG_031912.1:g.46744G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_002465.4:c.611G>C MANE Select	NP_002456.2:p.Gly204Ala
ENST00000361466.7:c.611G>C MANE Select	ENSP00000354849.2:p.Gly204Ala
NM_001254718.1:c.536G>C	NP_001241647.1:p.Gly179Ala
NM_001254718.2:c.536G>C	NP_001241647.1:p.Gly179Ala
NM_001254719.1:c.536G>C	NP_001241648.1:p.Gly179Ala
NM_001254719.2:c.536G>C	NP_001241648.1:p.Gly179Ala
NM_001254720.1:c.500G>C	NP_001241649.1:p.Gly167Ala
NM_001254720.2:c.500G>C	NP_001241649.1:p.Gly167Ala
NM_001254721.1:c.533+2069G>C	NP_001241650.1:n.533+2069G>C
NM_001254721.2:c.533+2069G>C	NP_001241650.1:n.533+2069G>C
NM_001254722.1:c.458G>C	NP_001241651.1:p.Gly153Ala
NM_001254722.2:c.458G>C	NP_001241651.1:p.Gly153Ala
NM_001254723.1:c.497G>C	NP_001241652.1:p.Gly166Ala
NM_001254723.2:c.497G>C	NP_001241652.1:p.Gly166Ala
NM_002465.3:c.611G>C	NP_002456.2:p.Gly204Ala
NM_206819.2:c.611G>C	NP_996555.1:p.Gly204Ala
NM_206819.3:c.611G>C	NP_996555.1:p.Gly204Ala
NM_206820.2:c.536G>C	NP_996556.1:p.Gly179Ala
NM_206820.3:c.536G>C	NP_996556.1:p.Gly179Ala
NM_206821.2:c.536G>C	NP_996557.1:p.Gly179Ala
NM_206821.3:c.536G>C	NP_996557.1:p.Gly179Ala
ENST00000361466.6:c.611G>C	ENSP00000354849.2:p.Gly204Ala
ENST00000361685.6:c.611G>C	ENSP00000354845.2:p.Gly204Ala
ENST00000392934.7:c.497G>C	ENSP00000376665.3:p.Gly166Ala
ENST00000441232.5:c.611G>C	ENSP00000388989.3:p.Gly204Ala
ENST00000452455.6:c.536G>C	ENSP00000400908.2:p.Gly179Ala
ENST00000536007.5:c.533+2069G>C	ENSP00000446128.1:n.533+2069G>C
ENST00000541119.5:c.500G>C	ENSP00000442847.1:p.Gly167Ala
ENST00000545503.6:c.536G>C	ENSP00000440034.2:p.Gly179Ala
ENST00000547405.5:c.458G>C	ENSP00000448175.1:p.Gly153Ala
ENST00000547509.5:c.494G>C	ENSP00000447362.1:p.Gly165Ala
ENST00000549145.5:c.575G>C	ENSP00000447660.1:p.Gly192Ala
ENST00000550270.1:c.536G>C	ENSP00000449702.1:p.Gly179Ala
ENST00000550312.5:n.492G>C
ENST00000550501.3:n.574+21730G>C
ENST00000550514.5:c.239G>C	ENSP00000447404.1:p.Gly80Ala
ENST00000551300.5:c.239G>C	ENSP00000447116.1:p.Gly80Ala
ENST00000552198.5:n.498G>C
ENST00000553190.5:c.536G>C	ENSP00000447900.1:p.Gly179Ala
XM_005268876.3:c.575G>C	XP_005268933.1:p.Gly192Ala
XM_005268876.4:c.575G>C	XP_005268933.1:p.Gly192Ala
XM_006719405.2:c.611G>C	XP_006719468.1:p.Gly204Ala
XM_006719405.4:c.611G>C	XP_006719468.1:p.Gly204Ala
XM_006719406.2:c.611G>C	XP_006719469.1:p.Gly204Ala
XM_006719406.4:c.611G>C	XP_006719469.1:p.Gly204Ala
XM_006719407.2:c.575G>C	XP_006719470.1:p.Gly192Ala
XM_006719407.3:c.575G>C	XP_006719470.1:p.Gly192Ala
XM_006719408.2:c.611G>C	XP_006719471.1:p.Gly204Ala
XM_006719408.4:c.611G>C	XP_006719471.1:p.Gly204Ala
XM_006719409.2:c.536G>C	XP_006719472.1:p.Gly179Ala
XM_006719409.3:c.536G>C	XP_006719472.1:p.Gly179Ala
XM_006719410.2:c.611G>C	XP_006719473.1:p.Gly204Ala
XM_006719410.4:c.611G>C	XP_006719473.1:p.Gly204Ala
XM_006719411.2:c.536G>C	XP_006719474.1:p.Gly179Ala
XM_006719411.3:c.536G>C	XP_006719474.1:p.Gly179Ala
XM_017019315.2:c.608+2069G>C	XP_016874804.1:n.608+2069G>C
XM_017019316.2:c.611G>C	XP_016874805.1:p.Gly204Ala
XM_017019317.1:c.536G>C	XP_016874806.1:p.Gly179Ala
XM_017019318.2:c.608+2069G>C	XP_016874807.1:n.608+2069G>C
XM_017019319.2:c.533+2069G>C	XP_016874808.1:n.533+2069G>C
XM_017019320.1:c.458G>C	XP_016874809.1:p.Gly153Ala
XM_017019321.2:c.533+2069G>C	XP_016874810.1:n.533+2069G>C
XM_017019322.1:c.455+2069G>C	XP_016874811.1:n.455+2069G>C