Canonical Allele Identifier: CA422807488

Gene: ASPM

Linked Data

• dbSNP Id: rs1445915977
• gnomAD v2: 1-197073347-T-C
• gnomAD v3: 1-197104217-T-C
• gnomAD v4: 1-197104217-T-C
• MyVariant Identifiers: chr1:g.197073347T>C (hg19) ; chr1:g.197104217T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197104217T>C , CM000663.2:g.197104217T>C	GRCh38
NC_000001.10:g.197073347T>C , CM000663.1:g.197073347T>C	GRCh37
NC_000001.9:g.195339970T>C	NCBI36
NG_015867.1:g.47478A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-8053A>G
ENST00000367409.9:c.5034A>G MANE Select	ENSP00000356379.4:p.Leu1678=
ENST00000680265.1:c.5034A>G	ENSP00000505384.1:p.Leu1678=
ENST00000680710.1:c.5034A>G	ENSP00000506676.1:p.Leu1678=
ENST00000294732.11:c.4066-8053A>G	ENSP00000294732.7:n.4066-8053A>G
ENST00000367408.5:c.1816-8053A>G	ENSP00000356378.1:n.1816-8053A>G
ENST00000367409.8:c.5034A>G	ENSP00000356379.4:p.Leu1678=
ENST00000612785.1:c.562-1570A>G	ENSP00000479244.1:n.562-1570A>G
NM_001206846.1:c.4066-8053A>G	NP_001193775.1:n.4066-8053A>G
NM_018136.4:c.5034A>G	NP_060606.3:p.Leu1678=
NM_018136.5:c.5034A>G MANE Select	NP_060606.3:p.Leu1678=
NM_001206846.2:c.4066-8053A>G	NP_001193775.1:n.4066-8053A>G