Canonical Allele Identifier: CA35862190

Gene: ASPM

Linked Data

• dbSNP Id: rs957152605
• MyVariant Identifiers: chr1:g.197060028G>T (hg19) ; chr1:g.197090898G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090898G>T , CM000663.2:g.197090898G>T	GRCh38
NC_000001.10:g.197060028G>T , CM000663.1:g.197060028G>T	GRCh37
NC_000001.9:g.195326651G>T	NCBI36
NG_015867.1:g.60797C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2875C>A
ENST00000367409.9:c.9588C>A MANE Select	ENSP00000356379.4:p.Leu3196=
ENST00000680265.1:c.9810C>A	ENSP00000505384.1:p.Leu3270=
ENST00000680710.1:c.9564C>A	ENSP00000506676.1:p.Leu3188=
ENST00000294732.11:c.4833C>A	ENSP00000294732.7:p.Leu1611=
ENST00000367408.5:c.2583C>A	ENSP00000356378.1:p.Leu861=
ENST00000367409.8:c.9588C>A	ENSP00000356379.4:p.Leu3196=
ENST00000612785.1:c.3546C>A	ENSP00000479244.1:p.Leu1182=
NM_001206846.1:c.4833C>A	NP_001193775.1:p.Leu1611=
NM_018136.4:c.9588C>A	NP_060606.3:p.Leu3196=
NM_018136.5:c.9588C>A MANE Select	NP_060606.3:p.Leu3196=
NM_001206846.2:c.4833C>A	NP_001193775.1:p.Leu1611=