Canonical Allele Identifier: CA149006

Gene: ASPM

Linked Data

• ClinVar Variation Id: 95889
• ClinVar RCV Id: RCV000081937 ; RCV000391426 ; RCV000710081 ; RCV003915096
• dbSNP Id: rs41299623
• ExAC: 1:197073196 G / A
• gnomAD v2: 1-197073196-G-A
• gnomAD v3: 1-197104066-G-A
• gnomAD v4: 1-197104066-G-A
• MyVariant Identifiers: chr1:g.197073196G>A (hg19) ; chr1:g.197104066G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197104066G>A , CM000663.2:g.197104066G>A	GRCh38
NC_000001.10:g.197073196G>A , CM000663.1:g.197073196G>A	GRCh37
NC_000001.9:g.195339819G>A	NCBI36
NG_015867.1:g.47629C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-7902C>T
ENST00000367409.9:c.5185C>T MANE Select	ENSP00000356379.4:p.Arg1729Trp
ENST00000680265.1:c.5185C>T	ENSP00000505384.1:p.Arg1729Trp
ENST00000680710.1:c.5185C>T	ENSP00000506676.1:p.Arg1729Trp
ENST00000294732.11:c.4066-7902C>T	ENSP00000294732.7:n.4066-7902C>T
ENST00000367408.5:c.1816-7902C>T	ENSP00000356378.1:n.1816-7902C>T
ENST00000367409.8:c.5185C>T	ENSP00000356379.4:p.Arg1729Trp
ENST00000612785.1:c.562-1419C>T	ENSP00000479244.1:n.562-1419C>T
NM_001206846.1:c.4066-7902C>T	NP_001193775.1:n.4066-7902C>T
NM_018136.4:c.5185C>T	NP_060606.3:p.Arg1729Trp
NM_018136.5:c.5185C>T MANE Select	NP_060606.3:p.Arg1729Trp
NM_001206846.2:c.4066-7902C>T	NP_001193775.1:n.4066-7902C>T