Canonical Allele Identifier: CA344001758

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059398T>A (hg19) ; chr1:g.197090268T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090268T>A , CM000663.2:g.197090268T>A	GRCh38
NC_000001.10:g.197059398T>A , CM000663.1:g.197059398T>A	GRCh37
NC_000001.9:g.195326021T>A	NCBI36
NG_015867.1:g.61427A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3044A>T
ENST00000367409.9:c.9757A>T MANE Select	ENSP00000356379.4:p.Thr3253Ser
ENST00000680265.1:c.9979A>T	ENSP00000505384.1:p.Thr3327Ser
ENST00000680710.1:c.9733A>T	ENSP00000506676.1:p.Thr3245Ser
ENST00000294732.11:c.5002A>T	ENSP00000294732.7:p.Thr1668Ser
ENST00000367408.5:c.2752A>T	ENSP00000356378.1:p.Thr918Ser
ENST00000367409.8:c.9757A>T	ENSP00000356379.4:p.Thr3253Ser
ENST00000612785.1:c.3715A>T	ENSP00000479244.1:p.Thr1239Ser
NM_001206846.1:c.5002A>T	NP_001193775.1:p.Thr1668Ser
NM_018136.4:c.9757A>T	NP_060606.3:p.Thr3253Ser
NM_018136.5:c.9757A>T MANE Select	NP_060606.3:p.Thr3253Ser
NM_001206846.2:c.5002A>T	NP_001193775.1:p.Thr1668Ser