Canonical Allele Identifier: CA1760939367

Gene: MCPH1

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.6494838G= , CM000670.2:g.6494838G=	GRCh38
NC_000008.10:g.6352359G= , CM000670.1:g.6352359G=	GRCh37
NC_000008.9:g.6339767G=	NCBI36
NG_016619.1:g.93247G=
NG_016619.2:g.93247G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000519221.6:n.363-5014G=
ENST00000521129.2:c.184-5014G=	ENSP00000509664.1:n.184-5014G=
ENST00000521175.2:n.860-5014G=
ENST00000687324.1:n.1075-5014G=
ENST00000687413.1:c.226-5014G=	ENSP00000510583.1:n.226-5014G=
ENST00000687720.1:c.*2085-5014G=	ENSP00000510728.1:n.*2085-5014G=
ENST00000688101.1:c.2294-5014G=
ENST00000688388.1:c.*126-5014G=	ENSP00000510092.1:n.*126-5014G=
ENST00000688912.1:n.2148-5014G=
ENST00000689148.1:n.1097-5014G=
ENST00000689348.1:c.2137-5014G=	ENSP00000509554.1:n.2137-5014G=
ENST00000689633.1:c.1935+39586G=	ENSP00000509054.1:n.1935+39586G=
ENST00000689736.1:c.781-5014G=	ENSP00000509722.1:n.781-5014G=
ENST00000690159.1:c.*2416-5014G=	ENSP00000510482.1:n.*2416-5014G=
ENST00000690708.1:c.982-5014G=	ENSP00000510400.1:n.982-5014G=
ENST00000690826.1:c.2137-5014G=	ENSP00000510536.1:n.2137-5014G=
ENST00000691435.1:c.2137-5014G=	ENSP00000510652.1:n.2137-5014G=
ENST00000691655.1:c.*1074-5014G=	ENSP00000509652.1:n.*1074-5014G=
ENST00000692836.1:c.2137-5014G=	ENSP00000509971.1:n.2137-5014G=
ENST00000692938.1:c.2137-5014G=	ENSP00000509072.1:n.2137-5014G=
ENST00000693231.1:c.*1675+39586G=	ENSP00000510764.1:n.*1675+39586G=
ENST00000344683.10:c.2137-5014G= MANE Select	ENSP00000342924.5:n.2137-5014G=
ENST00000344683.9:c.2137-5014G=	ENSP00000342924.5:n.2137-5014G=
ENST00000519221.5:n.244-5014G=
ENST00000521129.1:n.295-5014G=
NM_024596.3:c.2137-5014G=	NP_078872.2:n.2137-5014G=
XM_011534755.1:c.2137-5014G=	XP_011533057.1:n.2137-5014G=
XM_011534756.1:c.2137-5014G=	XP_011533058.1:n.2137-5014G=
XM_011534757.1:c.2137-5014G=	XP_011533059.1:n.2137-5014G=
XM_011534758.1:c.2137-5014G=	XP_011533060.1:n.2137-5014G=
XM_011534759.1:c.2137-5014G=	XP_011533061.1:n.2137-5014G=
XM_011534760.1:c.1612-5014G=	XP_011533062.1:n.1612-5014G=
NM_001322042.1:c.2137-5014G=	NP_001308971.1:n.2137-5014G=
NM_001363979.1:c.2137-5014G=	NP_001350908.1:n.2137-5014G=
NM_001363980.1:c.1935+39586G=	NP_001350909.1:n.1935+39586G=
NM_024596.4:c.2137-5014G=	NP_078872.2:n.2137-5014G=
XM_011534755.3:c.2137-5014G=	XP_011533057.1:n.2137-5014G=
XM_011534756.3:c.2137-5014G=	XP_011533058.1:n.2137-5014G=
XM_011534757.3:c.2137-5014G=	XP_011533059.1:n.2137-5014G=
XM_011534758.3:c.2137-5014G=	XP_011533060.1:n.2137-5014G=
XM_011534759.3:c.2137-5014G=	XP_011533061.1:n.2137-5014G=
XM_011534760.2:c.1612-5014G=	XP_011533062.1:n.1612-5014G=
XM_017013829.2:c.2137-5014G=	XP_016869318.1:n.2137-5014G=
XM_017013831.2:c.1936-5014G=	XP_016869320.1:n.1936-5014G=
XM_017013832.2:c.1935+39586G=	XP_016869321.1:n.1935+39586G=
XM_017013833.2:c.2137-5014G=	XP_016869322.1:n.2137-5014G=
XR_001745596.2:n.2190-5014G=
NM_024596.5:c.2137-5014G= MANE Select	NP_078872.3:n.2137-5014G=
NM_001322042.2:c.2137-5014G=	NP_001308971.2:n.2137-5014G=
NM_001363980.2:c.1935+39586G=	NP_001350909.1:n.1935+39586G=