Canonical Allele Identifier: CA370221362

Gene: MCPH1

Linked Data

• ClinVar Variation Id: 1973872
• ClinVar RCV Id: RCV002736332
• gnomAD v4: 8-6445028-C-T
• MyVariant Identifiers: chr8:g.6302549C>T (hg19) ; chr8:g.6445028C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.6445028C>T , CM000670.2:g.6445028C>T	GRCh38
NC_000008.10:g.6302549C>T , CM000670.1:g.6302549C>T	GRCh37
NC_000008.9:g.6289957C>T	NCBI36
NG_016619.1:g.43437C>T
NG_016619.2:g.43437C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000519480.6:c.1306C>T	ENSP00000430962.1:p.Pro436Ser
ENST00000685179.1:c.1300C>T	ENSP00000510001.1:p.Pro434Ser
ENST00000686750.1:c.1216C>T	ENSP00000509053.1:p.Pro406Ser
ENST00000687577.1:n.2867C>T
ENST00000687720.1:c.*1254C>T	ENSP00000510728.1:n.*1254C>T
ENST00000687874.1:n.685+2872C>T
ENST00000688099.1:c.*1585C>T	ENSP00000509622.1:n.*1585C>T
ENST00000688101.1:c.726C>T
ENST00000688388.1:c.1306C>T	ENSP00000510092.1:p.Pro436Ser
ENST00000688452.1:c.*825C>T	ENSP00000510556.1:n.*825C>T
ENST00000688658.1:n.146C>T
ENST00000688912.1:n.1317C>T
ENST00000689348.1:c.1306C>T	ENSP00000509554.1:p.Pro436Ser
ENST00000689633.1:c.1306C>T	ENSP00000509054.1:p.Pro436Ser
ENST00000689736.1:c.670+2872C>T	ENSP00000509722.1:n.670+2872C>T
ENST00000690159.1:c.*1585C>T	ENSP00000510482.1:n.*1585C>T
ENST00000690518.1:c.*1046C>T	ENSP00000509135.1:n.*1046C>T
ENST00000690682.1:c.*1201C>T	ENSP00000509896.1:n.*1201C>T
ENST00000690708.1:c.670+2872C>T	ENSP00000510400.1:n.670+2872C>T
ENST00000690826.1:c.1306C>T	ENSP00000510536.1:p.Pro436Ser
ENST00000691435.1:c.1306C>T	ENSP00000510652.1:p.Pro436Ser
ENST00000691655.1:c.*680+2872C>T	ENSP00000509652.1:n.*680+2872C>T
ENST00000691738.1:n.1514C>T
ENST00000692534.1:c.203+523C>T
ENST00000692836.1:c.1306C>T	ENSP00000509971.1:p.Pro436Ser
ENST00000692938.1:c.1306C>T	ENSP00000509072.1:p.Pro436Ser
ENST00000693231.1:c.*1046C>T	ENSP00000510764.1:n.*1046C>T
ENST00000344683.10:c.1306C>T MANE Select	ENSP00000342924.5:p.Pro436Ser
ENST00000344683.9:c.1306C>T	ENSP00000342924.5:p.Pro436Ser
ENST00000519480.5:c.1306C>T	ENSP00000430962.1:p.Pro436Ser
ENST00000522905.1:c.1162C>T	ENSP00000430768.1:p.Pro388Ser
NM_001172574.1:c.1306C>T	NP_001166045.1:p.Pro436Ser
NM_001172575.1:c.1162C>T	NP_001166046.1:p.Pro388Ser
NM_024596.3:c.1306C>T	NP_078872.2:p.Pro436Ser
XM_011534755.1:c.1306C>T	XP_011533057.1:p.Pro436Ser
XM_011534756.1:c.1306C>T	XP_011533058.1:p.Pro436Ser
XM_011534757.1:c.1306C>T	XP_011533059.1:p.Pro436Ser
XM_011534758.1:c.1306C>T	XP_011533060.1:p.Pro436Ser
XM_011534759.1:c.1306C>T	XP_011533061.1:p.Pro436Ser
XM_011534760.1:c.781C>T	XP_011533062.1:p.Pro261Ser
NM_001322042.1:c.1306C>T	NP_001308971.1:p.Pro436Ser
NM_001322043.1:c.1300C>T	NP_001308972.1:p.Pro434Ser
NM_001322045.1:c.1204C>T	NP_001308974.1:p.Pro402Ser
NM_001363979.1:c.1306C>T	NP_001350908.1:p.Pro436Ser
NM_001363980.1:c.1306C>T	NP_001350909.1:p.Pro436Ser
NM_024596.4:c.1306C>T	NP_078872.2:p.Pro436Ser
NR_136159.1:n.1267C>T
XM_011534755.3:c.1306C>T	XP_011533057.1:p.Pro436Ser
XM_011534756.3:c.1306C>T	XP_011533058.1:p.Pro436Ser
XM_011534757.3:c.1306C>T	XP_011533059.1:p.Pro436Ser
XM_011534758.3:c.1306C>T	XP_011533060.1:p.Pro436Ser
XM_011534759.3:c.1306C>T	XP_011533061.1:p.Pro436Ser
XM_011534760.2:c.781C>T	XP_011533062.1:p.Pro261Ser
XM_017013829.2:c.1306C>T	XP_016869318.1:p.Pro436Ser
XM_017013831.2:c.1306C>T	XP_016869320.1:p.Pro436Ser
XM_017013832.2:c.1306C>T	XP_016869321.1:p.Pro436Ser
XM_017013833.2:c.1306C>T	XP_016869322.1:p.Pro436Ser
XR_001745596.2:n.1359C>T
NM_024596.5:c.1306C>T MANE Select	NP_078872.3:p.Pro436Ser
NM_001322042.2:c.1306C>T	NP_001308971.2:p.Pro436Ser
NM_001363980.2:c.1306C>T	NP_001350909.1:p.Pro436Ser
NM_001172574.2:c.1306C>T	NP_001166045.2:p.Pro436Ser
NM_001172575.2:c.1162C>T	NP_001166046.1:p.Pro388Ser
NM_001322043.2:c.1300C>T	NP_001308972.2:p.Pro434Ser
NM_001322045.2:c.1204C>T	NP_001308974.2:p.Pro402Ser
NR_136159.2:n.1232C>T