Canonical Allele Identifier: CA343998826

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057559C>A (hg19) ; chr1:g.197088429C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088429C>A , CM000663.2:g.197088429C>A	GRCh38
NC_000001.10:g.197057559C>A , CM000663.1:g.197057559C>A	GRCh37
NC_000001.9:g.195324182C>A	NCBI36
NG_015867.1:g.63266G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3275G>T
ENST00000367409.9:c.9988G>T MANE Select	ENSP00000356379.4:p.Glu3330Ter
ENST00000680265.1:c.10210G>T	ENSP00000505384.1:p.Glu3404Ter
ENST00000680710.1:c.9964G>T	ENSP00000506676.1:p.Glu3322Ter
ENST00000294732.11:c.5233G>T	ENSP00000294732.7:p.Glu1745Ter
ENST00000367408.5:c.2983G>T	ENSP00000356378.1:p.Glu995Ter
ENST00000367409.8:c.9988G>T	ENSP00000356379.4:p.Glu3330Ter
ENST00000612785.1:c.3946G>T	ENSP00000479244.1:p.Glu1316Ter
NM_001206846.1:c.5233G>T	NP_001193775.1:p.Glu1745Ter
NM_018136.4:c.9988G>T	NP_060606.3:p.Glu3330Ter
NM_018136.5:c.9988G>T MANE Select	NP_060606.3:p.Glu3330Ter
NM_001206846.2:c.5233G>T	NP_001193775.1:p.Glu1745Ter