Canonical Allele Identifier: CA277095

Gene: ASPM

Linked Data

• ClinVar Variation Id: 210358
• ClinVar RCV Id: RCV000193186
• dbSNP Id: rs797045314
• MyVariant Identifiers: chr1:g.197072849A>C (hg19) ; chr1:g.197103719A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103719A>C , CM000663.2:g.197103719A>C	GRCh38
NC_000001.10:g.197072849A>C , CM000663.1:g.197072849A>C	GRCh37
NC_000001.9:g.195339472A>C	NCBI36
NG_015867.1:g.47976T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7555T>G
ENST00000367409.9:c.5532T>G MANE Select	ENSP00000356379.4:p.Tyr1844Ter
ENST00000680265.1:c.5532T>G	ENSP00000505384.1:p.Tyr1844Ter
ENST00000680710.1:c.5532T>G	ENSP00000506676.1:p.Tyr1844Ter
ENST00000294732.11:c.4066-7555T>G	ENSP00000294732.7:n.4066-7555T>G
ENST00000367408.5:c.1816-7555T>G	ENSP00000356378.1:n.1816-7555T>G
ENST00000367409.8:c.5532T>G	ENSP00000356379.4:p.Tyr1844Ter
ENST00000612785.1:c.562-1072T>G	ENSP00000479244.1:n.562-1072T>G
NM_001206846.1:c.4066-7555T>G	NP_001193775.1:n.4066-7555T>G
NM_018136.4:c.5532T>G	NP_060606.3:p.Tyr1844Ter
NM_018136.5:c.5532T>G MANE Select	NP_060606.3:p.Tyr1844Ter
NM_001206846.2:c.4066-7555T>G	NP_001193775.1:n.4066-7555T>G