Canonical Allele Identifier: CA459598269

Gene: MCPH1

Linked Data

• MyVariant Identifiers: chr8:g.6302554A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.6445033A>G , CM000670.2:g.6445033A>G	GRCh38
NC_000008.10:g.6302554A>G , CM000670.1:g.6302554A>G	GRCh37
NC_000008.9:g.6289962A>G	NCBI36
NG_016619.1:g.43442A>G
NG_016619.2:g.43442A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000519480.6:c.1311A>G	ENSP00000430962.1:p.Ser437=
ENST00000685179.1:c.1305A>G	ENSP00000510001.1:p.Ser435=
ENST00000686750.1:c.1221A>G	ENSP00000509053.1:p.Ser407=
ENST00000687577.1:n.2872A>G
ENST00000687720.1:c.*1259A>G	ENSP00000510728.1:n.*1259A>G
ENST00000687874.1:n.685+2877A>G
ENST00000688099.1:c.*1590A>G	ENSP00000509622.1:n.*1590A>G
ENST00000688101.1:c.731A>G
ENST00000688388.1:c.1311A>G	ENSP00000510092.1:p.Ser437=
ENST00000688452.1:c.*830A>G	ENSP00000510556.1:n.*830A>G
ENST00000688658.1:n.151A>G
ENST00000688912.1:n.1322A>G
ENST00000689348.1:c.1311A>G	ENSP00000509554.1:p.Ser437=
ENST00000689633.1:c.1311A>G	ENSP00000509054.1:p.Ser437=
ENST00000689736.1:c.670+2877A>G	ENSP00000509722.1:n.670+2877A>G
ENST00000690159.1:c.*1590A>G	ENSP00000510482.1:n.*1590A>G
ENST00000690518.1:c.*1051A>G	ENSP00000509135.1:n.*1051A>G
ENST00000690682.1:c.*1206A>G	ENSP00000509896.1:n.*1206A>G
ENST00000690708.1:c.670+2877A>G	ENSP00000510400.1:n.670+2877A>G
ENST00000690826.1:c.1311A>G	ENSP00000510536.1:p.Ser437=
ENST00000691435.1:c.1311A>G	ENSP00000510652.1:p.Ser437=
ENST00000691655.1:c.*680+2877A>G	ENSP00000509652.1:n.*680+2877A>G
ENST00000691738.1:n.1519A>G
ENST00000692534.1:c.203+528A>G
ENST00000692836.1:c.1311A>G	ENSP00000509971.1:p.Ser437=
ENST00000692938.1:c.1311A>G	ENSP00000509072.1:p.Ser437=
ENST00000693231.1:c.*1051A>G	ENSP00000510764.1:n.*1051A>G
ENST00000344683.10:c.1311A>G MANE Select	ENSP00000342924.5:p.Ser437=
ENST00000344683.9:c.1311A>G	ENSP00000342924.5:p.Ser437=
ENST00000519480.5:c.1311A>G	ENSP00000430962.1:p.Ser437=
ENST00000522905.1:c.1167A>G	ENSP00000430768.1:p.Ser389=
NM_001172574.1:c.1311A>G	NP_001166045.1:p.Ser437=
NM_001172575.1:c.1167A>G	NP_001166046.1:p.Ser389=
NM_024596.3:c.1311A>G	NP_078872.2:p.Ser437=
XM_011534755.1:c.1311A>G	XP_011533057.1:p.Ser437=
XM_011534756.1:c.1311A>G	XP_011533058.1:p.Ser437=
XM_011534757.1:c.1311A>G	XP_011533059.1:p.Ser437=
XM_011534758.1:c.1311A>G	XP_011533060.1:p.Ser437=
XM_011534759.1:c.1311A>G	XP_011533061.1:p.Ser437=
XM_011534760.1:c.786A>G	XP_011533062.1:p.Ser262=
NM_001322042.1:c.1311A>G	NP_001308971.1:p.Ser437=
NM_001322043.1:c.1305A>G	NP_001308972.1:p.Ser435=
NM_001322045.1:c.1209A>G	NP_001308974.1:p.Ser403=
NM_001363979.1:c.1311A>G	NP_001350908.1:p.Ser437=
NM_001363980.1:c.1311A>G	NP_001350909.1:p.Ser437=
NM_024596.4:c.1311A>G	NP_078872.2:p.Ser437=
NR_136159.1:n.1272A>G
XM_011534755.3:c.1311A>G	XP_011533057.1:p.Ser437=
XM_011534756.3:c.1311A>G	XP_011533058.1:p.Ser437=
XM_011534757.3:c.1311A>G	XP_011533059.1:p.Ser437=
XM_011534758.3:c.1311A>G	XP_011533060.1:p.Ser437=
XM_011534759.3:c.1311A>G	XP_011533061.1:p.Ser437=
XM_011534760.2:c.786A>G	XP_011533062.1:p.Ser262=
XM_017013829.2:c.1311A>G	XP_016869318.1:p.Ser437=
XM_017013831.2:c.1311A>G	XP_016869320.1:p.Ser437=
XM_017013832.2:c.1311A>G	XP_016869321.1:p.Ser437=
XM_017013833.2:c.1311A>G	XP_016869322.1:p.Ser437=
XR_001745596.2:n.1364A>G
NM_024596.5:c.1311A>G MANE Select	NP_078872.3:p.Ser437=
NM_001322042.2:c.1311A>G	NP_001308971.2:p.Ser437=
NM_001363980.2:c.1311A>G	NP_001350909.1:p.Ser437=
NM_001172574.2:c.1311A>G	NP_001166045.2:p.Ser437=
NM_001172575.2:c.1167A>G	NP_001166046.1:p.Ser389=
NM_001322043.2:c.1305A>G	NP_001308972.2:p.Ser435=
NM_001322045.2:c.1209A>G	NP_001308974.2:p.Ser403=
NR_136159.2:n.1237A>G