Canonical Allele Identifier: CA344017171

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197112168C>A (hg19) ; chr1:g.197143038C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197143038C>A , CM000663.2:g.197143038C>A	GRCh38
NC_000001.10:g.197112168C>A , CM000663.1:g.197112168C>A	GRCh37
NC_000001.9:g.195378791C>A	NCBI36
NG_015867.1:g.8657G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1214G>T MANE Select	ENSP00000356379.4:p.Cys405Phe
ENST00000679766.1:n.1431G>T
ENST00000680265.1:c.1214G>T	ENSP00000505384.1:p.Cys405Phe
ENST00000680710.1:c.1214G>T	ENSP00000506676.1:p.Cys405Phe
ENST00000681879.1:c.1214G>T	ENSP00000505363.1:p.Cys405Phe
ENST00000294732.11:c.1214G>T	ENSP00000294732.7:p.Cys405Phe
ENST00000367409.8:c.1214G>T	ENSP00000356379.4:p.Cys405Phe
ENST00000612785.1:c.561+653G>T	ENSP00000479244.1:n.561+653G>T
NM_001206846.1:c.1214G>T	NP_001193775.1:p.Cys405Phe
NM_018136.4:c.1214G>T	NP_060606.3:p.Cys405Phe
NM_018136.5:c.1214G>T MANE Select	NP_060606.3:p.Cys405Phe
NM_001206846.2:c.1214G>T	NP_001193775.1:p.Cys405Phe