Canonical Allele Identifier: CA344001912

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059469A>G (hg19) ; chr1:g.197090339A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090339A>G , CM000663.2:g.197090339A>G	GRCh38
NC_000001.10:g.197059469A>G , CM000663.1:g.197059469A>G	GRCh37
NC_000001.9:g.195326092A>G	NCBI36
NG_015867.1:g.61356T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2973T>C
ENST00000367409.9:c.9686T>C MANE Select	ENSP00000356379.4:p.Ile3229Thr
ENST00000680265.1:c.9908T>C	ENSP00000505384.1:p.Ile3303Thr
ENST00000680710.1:c.9662T>C	ENSP00000506676.1:p.Ile3221Thr
ENST00000294732.11:c.4931T>C	ENSP00000294732.7:p.Ile1644Thr
ENST00000367408.5:c.2681T>C	ENSP00000356378.1:p.Ile894Thr
ENST00000367409.8:c.9686T>C	ENSP00000356379.4:p.Ile3229Thr
ENST00000612785.1:c.3644T>C	ENSP00000479244.1:p.Ile1215Thr
NM_001206846.1:c.4931T>C	NP_001193775.1:p.Ile1644Thr
NM_018136.4:c.9686T>C	NP_060606.3:p.Ile3229Thr
NM_018136.5:c.9686T>C MANE Select	NP_060606.3:p.Ile3229Thr
NM_001206846.2:c.4931T>C	NP_001193775.1:p.Ile1644Thr