Canonical Allele Identifier: CA344026264

Gene: ASPM

Linked Data

• ClinVar Variation Id: 1360915
• ClinVar RCV Id: RCV001874189
• dbSNP Id: rs1657287577
• MyVariant Identifiers: chr1:g.197072805C>G (hg19) ; chr1:g.197103675C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197103675C>G , CM000663.2:g.197103675C>G	GRCh38
NC_000001.10:g.197072805C>G , CM000663.1:g.197072805C>G	GRCh37
NC_000001.9:g.195339428C>G	NCBI36
NG_015867.1:g.48020G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7511G>C
ENST00000367409.9:c.5576G>C MANE Select	ENSP00000356379.4:p.Arg1859Thr
ENST00000680265.1:c.5576G>C	ENSP00000505384.1:p.Arg1859Thr
ENST00000680710.1:c.5576G>C	ENSP00000506676.1:p.Arg1859Thr
ENST00000294732.11:c.4066-7511G>C	ENSP00000294732.7:n.4066-7511G>C
ENST00000367408.5:c.1816-7511G>C	ENSP00000356378.1:n.1816-7511G>C
ENST00000367409.8:c.5576G>C	ENSP00000356379.4:p.Arg1859Thr
ENST00000612785.1:c.562-1028G>C	ENSP00000479244.1:n.562-1028G>C
NM_001206846.1:c.4066-7511G>C	NP_001193775.1:n.4066-7511G>C
NM_018136.4:c.5576G>C	NP_060606.3:p.Arg1859Thr
NM_018136.5:c.5576G>C MANE Select	NP_060606.3:p.Arg1859Thr
NM_001206846.2:c.4066-7511G>C	NP_001193775.1:n.4066-7511G>C