Canonical Allele Identifier: CA343998099

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057471T>G (hg19) ; chr1:g.197088341T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088341T>G , CM000663.2:g.197088341T>G	GRCh38
NC_000001.10:g.197057471T>G , CM000663.1:g.197057471T>G	GRCh37
NC_000001.9:g.195324094T>G	NCBI36
NG_015867.1:g.63354A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3363A>C
ENST00000367409.9:c.10076A>C MANE Select	ENSP00000356379.4:p.Asn3359Thr
ENST00000680265.1:c.10298A>C	ENSP00000505384.1:p.Asn3433Thr
ENST00000680710.1:c.10052A>C	ENSP00000506676.1:p.Asn3351Thr
ENST00000294732.11:c.5321A>C	ENSP00000294732.7:p.Asn1774Thr
ENST00000367408.5:c.3071A>C	ENSP00000356378.1:p.Asn1024Thr
ENST00000367409.8:c.10076A>C	ENSP00000356379.4:p.Asn3359Thr
ENST00000612785.1:c.4034A>C	ENSP00000479244.1:p.Asn1345Thr
NM_001206846.1:c.5321A>C	NP_001193775.1:p.Asn1774Thr
NM_018136.4:c.10076A>C	NP_060606.3:p.Asn3359Thr
NM_018136.5:c.10076A>C MANE Select	NP_060606.3:p.Asn3359Thr
NM_001206846.2:c.5321A>C	NP_001193775.1:p.Asn1774Thr