Canonical Allele Identifier: CA422672224

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057521A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088391A>G , CM000663.2:g.197088391A>G	GRCh38
NC_000001.10:g.197057521A>G , CM000663.1:g.197057521A>G	GRCh37
NC_000001.9:g.195324144A>G	NCBI36
NG_015867.1:g.63304T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3313T>C
ENST00000367409.9:c.10026T>C MANE Select	ENSP00000356379.4:p.Cys3342=
ENST00000680265.1:c.10248T>C	ENSP00000505384.1:p.Cys3416=
ENST00000680710.1:c.10002T>C	ENSP00000506676.1:p.Cys3334=
ENST00000294732.11:c.5271T>C	ENSP00000294732.7:p.Cys1757=
ENST00000367408.5:c.3021T>C	ENSP00000356378.1:p.Cys1007=
ENST00000367409.8:c.10026T>C	ENSP00000356379.4:p.Cys3342=
ENST00000612785.1:c.3984T>C	ENSP00000479244.1:p.Cys1328=
NM_001206846.1:c.5271T>C	NP_001193775.1:p.Cys1757=
NM_018136.4:c.10026T>C	NP_060606.3:p.Cys3342=
NM_018136.5:c.10026T>C MANE Select	NP_060606.3:p.Cys3342=
NM_001206846.2:c.5271T>C	NP_001193775.1:p.Cys1757=