Canonical Allele Identifier: CA422806610
Gene: ASPM HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.197072105A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197102975A>G , CM000663.2:g.197102975A>G GRCh38
NC_000001.10:g.197072105A>G , CM000663.1:g.197072105A>G GRCh37
NC_000001.9:g.195338728A>G NCBI36
NG_015867.1:g.48720T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367408.6:n.2108-6811T>C
ENST00000367409.9:c.6276T>C MANE Select ENSP00000356379.4:p.Asn2092=
ENST00000680265.1:c.6276T>C ENSP00000505384.1:p.Asn2092=
ENST00000680710.1:c.6276T>C ENSP00000506676.1:p.Asn2092=
ENST00000294732.11:c.4066-6811T>C ENSP00000294732.7:n.4066-6811T>C
ENST00000367408.5:c.1816-6811T>C ENSP00000356378.1:n.1816-6811T>C
ENST00000367409.8:c.6276T>C ENSP00000356379.4:p.Asn2092=
ENST00000612785.1:c.562-328T>C ENSP00000479244.1:n.562-328T>C
NM_001206846.1:c.4066-6811T>C NP_001193775.1:n.4066-6811T>C
NM_018136.4:c.6276T>C NP_060606.3:p.Asn2092=
NM_018136.5:c.6276T>C MANE Select NP_060606.3:p.Asn2092=
NM_001206846.2:c.4066-6811T>C NP_001193775.1:n.4066-6811T>C