Canonical Allele Identifier: CA344006592

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197062187T>A (hg19) ; chr1:g.197093057T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093057T>A , CM000663.2:g.197093057T>A	GRCh38
NC_000001.10:g.197062187T>A , CM000663.1:g.197062187T>A	GRCh37
NC_000001.9:g.195328810T>A	NCBI36
NG_015867.1:g.58638A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2576A>T
ENST00000367409.9:c.9289A>T MANE Select	ENSP00000356379.4:p.Lys3097Ter
ENST00000680265.1:c.9511A>T	ENSP00000505384.1:p.Lys3171Ter
ENST00000680710.1:c.9289A>T	ENSP00000506676.1:p.Lys3097Ter
ENST00000294732.11:c.4534A>T	ENSP00000294732.7:p.Lys1512Ter
ENST00000367408.5:c.2284A>T	ENSP00000356378.1:p.Lys762Ter
ENST00000367409.8:c.9289A>T	ENSP00000356379.4:p.Lys3097Ter
ENST00000612785.1:c.3247A>T	ENSP00000479244.1:p.Lys1083Ter
NM_001206846.1:c.4534A>T	NP_001193775.1:p.Lys1512Ter
NM_018136.4:c.9289A>T	NP_060606.3:p.Lys3097Ter
NM_018136.5:c.9289A>T MANE Select	NP_060606.3:p.Lys3097Ter
NM_001206846.2:c.4534A>T	NP_001193775.1:p.Lys1512Ter