Canonical Allele Identifier: CA370223396

Gene: MCPH1

Linked Data

• MyVariant Identifiers: chr8:g.6312711G>T (hg19) ; chr8:g.6455190G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.6455190G>T , CM000670.2:g.6455190G>T	GRCh38
NC_000008.10:g.6312711G>T , CM000670.1:g.6312711G>T	GRCh37
NC_000008.9:g.6300119G>T	NCBI36
NG_016619.1:g.53599G>T
NG_016619.2:g.53599G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000687720.1:c.*1821G>T	ENSP00000510728.1:n.*1821G>T
ENST00000687874.1:n.733G>T
ENST00000688101.1:c.1293G>T
ENST00000688388.1:c.1873G>T	ENSP00000510092.1:p.Asp625Tyr
ENST00000688658.1:n.713G>T
ENST00000688912.1:n.1884G>T
ENST00000689348.1:c.1873G>T	ENSP00000509554.1:p.Asp625Tyr
ENST00000689633.1:c.1873G>T	ENSP00000509054.1:p.Asp625Tyr
ENST00000689736.1:c.718G>T	ENSP00000509722.1:p.Asp240Tyr
ENST00000690159.1:c.*2152G>T	ENSP00000510482.1:n.*2152G>T
ENST00000690708.1:c.718G>T	ENSP00000510400.1:p.Asp240Tyr
ENST00000690826.1:c.1873G>T	ENSP00000510536.1:p.Asp625Tyr
ENST00000691435.1:c.1873G>T	ENSP00000510652.1:p.Asp625Tyr
ENST00000691655.1:c.*728G>T	ENSP00000509652.1:n.*728G>T
ENST00000692534.1:c.251G>T
ENST00000692836.1:c.1873G>T	ENSP00000509971.1:p.Asp625Tyr
ENST00000692938.1:c.1873G>T	ENSP00000509072.1:p.Asp625Tyr
ENST00000693231.1:c.*1613G>T	ENSP00000510764.1:n.*1613G>T
ENST00000693528.1:n.106G>T
ENST00000344683.10:c.1873G>T MANE Select	ENSP00000342924.5:p.Asp625Tyr
ENST00000344683.9:c.1873G>T	ENSP00000342924.5:p.Asp625Tyr
NM_024596.3:c.1873G>T	NP_078872.2:p.Asp625Tyr
XM_011534755.1:c.1873G>T	XP_011533057.1:p.Asp625Tyr
XM_011534756.1:c.1873G>T	XP_011533058.1:p.Asp625Tyr
XM_011534757.1:c.1873G>T	XP_011533059.1:p.Asp625Tyr
XM_011534758.1:c.1873G>T	XP_011533060.1:p.Asp625Tyr
XM_011534759.1:c.1873G>T	XP_011533061.1:p.Asp625Tyr
XM_011534760.1:c.1348G>T	XP_011533062.1:p.Asp450Tyr
NM_001322042.1:c.1873G>T	NP_001308971.1:p.Asp625Tyr
NM_001363979.1:c.1873G>T	NP_001350908.1:p.Asp625Tyr
NM_001363980.1:c.1873G>T	NP_001350909.1:p.Asp625Tyr
NM_024596.4:c.1873G>T	NP_078872.2:p.Asp625Tyr
XM_011534755.3:c.1873G>T	XP_011533057.1:p.Asp625Tyr
XM_011534756.3:c.1873G>T	XP_011533058.1:p.Asp625Tyr
XM_011534757.3:c.1873G>T	XP_011533059.1:p.Asp625Tyr
XM_011534758.3:c.1873G>T	XP_011533060.1:p.Asp625Tyr
XM_011534759.3:c.1873G>T	XP_011533061.1:p.Asp625Tyr
XM_011534760.2:c.1348G>T	XP_011533062.1:p.Asp450Tyr
XM_017013829.2:c.1873G>T	XP_016869318.1:p.Asp625Tyr
XM_017013831.2:c.1873G>T	XP_016869320.1:p.Asp625Tyr
XM_017013832.2:c.1873G>T	XP_016869321.1:p.Asp625Tyr
XM_017013833.2:c.1873G>T	XP_016869322.1:p.Asp625Tyr
XR_001745596.2:n.1926G>T
NM_024596.5:c.1873G>T MANE Select	NP_078872.3:p.Asp625Tyr
NM_001322042.2:c.1873G>T	NP_001308971.2:p.Asp625Tyr
NM_001363980.2:c.1873G>T	NP_001350909.1:p.Asp625Tyr