Canonical Allele Identifier: CA422673136

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197062302G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093172G>A , CM000663.2:g.197093172G>A	GRCh38
NC_000001.10:g.197062302G>A , CM000663.1:g.197062302G>A	GRCh37
NC_000001.9:g.195328925G>A	NCBI36
NG_015867.1:g.58523C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2461C>T
ENST00000367409.9:c.9174C>T MANE Select	ENSP00000356379.4:p.Ile3058=
ENST00000680265.1:c.9396C>T	ENSP00000505384.1:p.Ile3132=
ENST00000680710.1:c.9174C>T	ENSP00000506676.1:p.Ile3058=
ENST00000294732.11:c.4419C>T	ENSP00000294732.7:p.Ile1473=
ENST00000367408.5:c.2169C>T	ENSP00000356378.1:p.Ile723=
ENST00000367409.8:c.9174C>T	ENSP00000356379.4:p.Ile3058=
ENST00000612785.1:c.3132C>T	ENSP00000479244.1:p.Ile1044=
NM_001206846.1:c.4419C>T	NP_001193775.1:p.Ile1473=
NM_018136.4:c.9174C>T	NP_060606.3:p.Ile3058=
NM_018136.5:c.9174C>T MANE Select	NP_060606.3:p.Ile3058=
NM_001206846.2:c.4419C>T	NP_001193775.1:p.Ile1473=