Canonical Allele Identifier: CA370221570
Gene: MCPH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1350408
ClinVar RCV Id: RCV002039720
dbSNP Id: rs1472912410
gnomAD v3: 8-6445124-A-T
gnomAD v4: 8-6445124-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.6445124A>T , CM000670.2:g.6445124A>T GRCh38
NC_000008.10:g.6302645A>T , CM000670.1:g.6302645A>T GRCh37
NC_000008.9:g.6290053A>T NCBI36
NG_016619.1:g.43533A>T
NG_016619.2:g.43533A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000519480.6:c.1402A>T ENSP00000430962.1:p.Thr468Ser
ENST00000685179.1:c.1396A>T ENSP00000510001.1:p.Thr466Ser
ENST00000686750.1:c.1312A>T ENSP00000509053.1:p.Thr438Ser
ENST00000687577.1:n.2963A>T
ENST00000687720.1:c.*1350A>T ENSP00000510728.1:n.*1350A>T
ENST00000687874.1:n.685+2968A>T
ENST00000688099.1:c.*1681A>T ENSP00000509622.1:n.*1681A>T
ENST00000688101.1:c.822A>T
ENST00000688388.1:c.1402A>T ENSP00000510092.1:p.Thr468Ser
ENST00000688452.1:c.*921A>T ENSP00000510556.1:n.*921A>T
ENST00000688658.1:n.242A>T
ENST00000688912.1:n.1413A>T
ENST00000689348.1:c.1402A>T ENSP00000509554.1:p.Thr468Ser
ENST00000689633.1:c.1402A>T ENSP00000509054.1:p.Thr468Ser
ENST00000689736.1:c.670+2968A>T ENSP00000509722.1:n.670+2968A>T
ENST00000690159.1:c.*1681A>T ENSP00000510482.1:n.*1681A>T
ENST00000690518.1:c.*1142A>T ENSP00000509135.1:n.*1142A>T
ENST00000690682.1:c.*1297A>T ENSP00000509896.1:n.*1297A>T
ENST00000690708.1:c.670+2968A>T ENSP00000510400.1:n.670+2968A>T
ENST00000690826.1:c.1402A>T ENSP00000510536.1:p.Thr468Ser
ENST00000691435.1:c.1402A>T ENSP00000510652.1:p.Thr468Ser
ENST00000691655.1:c.*680+2968A>T ENSP00000509652.1:n.*680+2968A>T
ENST00000691738.1:n.1610A>T
ENST00000692534.1:c.203+619A>T
ENST00000692836.1:c.1402A>T ENSP00000509971.1:p.Thr468Ser
ENST00000692938.1:c.1402A>T ENSP00000509072.1:p.Thr468Ser
ENST00000693231.1:c.*1142A>T ENSP00000510764.1:n.*1142A>T
ENST00000344683.10:c.1402A>T MANE Select ENSP00000342924.5:p.Thr468Ser
ENST00000344683.9:c.1402A>T ENSP00000342924.5:p.Thr468Ser
ENST00000519480.5:c.1402A>T ENSP00000430962.1:p.Thr468Ser
ENST00000522905.1:c.1258A>T ENSP00000430768.1:p.Thr420Ser
NM_001172574.1:c.1402A>T NP_001166045.1:p.Thr468Ser
NM_001172575.1:c.1258A>T NP_001166046.1:p.Thr420Ser
NM_024596.3:c.1402A>T NP_078872.2:p.Thr468Ser
XM_011534755.1:c.1402A>T XP_011533057.1:p.Thr468Ser
XM_011534756.1:c.1402A>T XP_011533058.1:p.Thr468Ser
XM_011534757.1:c.1402A>T XP_011533059.1:p.Thr468Ser
XM_011534758.1:c.1402A>T XP_011533060.1:p.Thr468Ser
XM_011534759.1:c.1402A>T XP_011533061.1:p.Thr468Ser
XM_011534760.1:c.877A>T XP_011533062.1:p.Thr293Ser
NM_001322042.1:c.1402A>T NP_001308971.1:p.Thr468Ser
NM_001322043.1:c.1396A>T NP_001308972.1:p.Thr466Ser
NM_001322045.1:c.1300A>T NP_001308974.1:p.Thr434Ser
NM_001363979.1:c.1402A>T NP_001350908.1:p.Thr468Ser
NM_001363980.1:c.1402A>T NP_001350909.1:p.Thr468Ser
NM_024596.4:c.1402A>T NP_078872.2:p.Thr468Ser
NR_136159.1:n.1363A>T
XM_011534755.3:c.1402A>T XP_011533057.1:p.Thr468Ser
XM_011534756.3:c.1402A>T XP_011533058.1:p.Thr468Ser
XM_011534757.3:c.1402A>T XP_011533059.1:p.Thr468Ser
XM_011534758.3:c.1402A>T XP_011533060.1:p.Thr468Ser
XM_011534759.3:c.1402A>T XP_011533061.1:p.Thr468Ser
XM_011534760.2:c.877A>T XP_011533062.1:p.Thr293Ser
XM_017013829.2:c.1402A>T XP_016869318.1:p.Thr468Ser
XM_017013831.2:c.1402A>T XP_016869320.1:p.Thr468Ser
XM_017013832.2:c.1402A>T XP_016869321.1:p.Thr468Ser
XM_017013833.2:c.1402A>T XP_016869322.1:p.Thr468Ser
XR_001745596.2:n.1455A>T
NM_024596.5:c.1402A>T MANE Select NP_078872.3:p.Thr468Ser
NM_001322042.2:c.1402A>T NP_001308971.2:p.Thr468Ser
NM_001363980.2:c.1402A>T NP_001350909.1:p.Thr468Ser
NM_001172574.2:c.1402A>T NP_001166045.2:p.Thr468Ser
NM_001172575.2:c.1258A>T NP_001166046.1:p.Thr420Ser
NM_001322043.2:c.1396A>T NP_001308972.2:p.Thr466Ser
NM_001322045.2:c.1300A>T NP_001308974.2:p.Thr434Ser
NR_136159.2:n.1328A>T