Canonical Allele Identifier: CA422674650

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197086931T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197117801T>C , CM000663.2:g.197117801T>C	GRCh38
NC_000001.10:g.197086931T>C , CM000663.1:g.197086931T>C	GRCh37
NC_000001.9:g.195353554T>C	NCBI36
NG_015867.1:g.33894A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2095A>G
ENST00000367409.9:c.4053A>G MANE Select	ENSP00000356379.4:p.Ala1351=
ENST00000680265.1:c.4053A>G	ENSP00000505384.1:p.Ala1351=
ENST00000680710.1:c.4053A>G	ENSP00000506676.1:p.Ala1351=
ENST00000681879.1:c.4101A>G	ENSP00000505363.1:n.4101A>G
ENST00000294732.11:c.4053A>G	ENSP00000294732.7:p.Ala1351=
ENST00000367408.5:c.1803A>G	ENSP00000356378.1:p.Ala601=
ENST00000367409.8:c.4053A>G	ENSP00000356379.4:p.Ala1351=
ENST00000612785.1:c.562-15154A>G	ENSP00000479244.1:n.562-15154A>G
NM_001206846.1:c.4053A>G	NP_001193775.1:p.Ala1351=
NM_018136.4:c.4053A>G	NP_060606.3:p.Ala1351=
NM_018136.5:c.4053A>G MANE Select	NP_060606.3:p.Ala1351=
NM_001206846.2:c.4053A>G	NP_001193775.1:p.Ala1351=