Canonical Allele Identifier: CA344003438

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060130C>A (hg19) ; chr1:g.197091000C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091000C>A , CM000663.2:g.197091000C>A	GRCh38
NC_000001.10:g.197060130C>A , CM000663.1:g.197060130C>A	GRCh37
NC_000001.9:g.195326753C>A	NCBI36
NG_015867.1:g.60695G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2773G>T
ENST00000367409.9:c.9486G>T MANE Select	ENSP00000356379.4:p.Gln3162His
ENST00000680265.1:c.9708G>T	ENSP00000505384.1:p.Gln3236His
ENST00000680710.1:c.9462G>T	ENSP00000506676.1:p.Gln3154His
ENST00000294732.11:c.4731G>T	ENSP00000294732.7:p.Gln1577His
ENST00000367408.5:c.2481G>T	ENSP00000356378.1:p.Gln827His
ENST00000367409.8:c.9486G>T	ENSP00000356379.4:p.Gln3162His
ENST00000612785.1:c.3444G>T	ENSP00000479244.1:p.Gln1148His
NM_001206846.1:c.4731G>T	NP_001193775.1:p.Gln1577His
NM_018136.4:c.9486G>T	NP_060606.3:p.Gln3162His
NM_018136.5:c.9486G>T MANE Select	NP_060606.3:p.Gln3162His
NM_001206846.2:c.4731G>T	NP_001193775.1:p.Gln1577His