Canonical Allele Identifier: CA1308856

Gene: ASPM

Linked Data

• dbSNP Id: rs762484822
• ExAC: 1:197059292 A / C
• gnomAD v2: 1-197059292-A-C
• MyVariant Identifiers: chr1:g.197059292A>C (hg19) ; chr1:g.197090162A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090162A>C , CM000663.2:g.197090162A>C	GRCh38
NC_000001.10:g.197059292A>C , CM000663.1:g.197059292A>C	GRCh37
NC_000001.9:g.195325915A>C	NCBI36
NG_015867.1:g.61533T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3116+34T>G
ENST00000367409.9:c.9829+34T>G MANE Select	ENSP00000356379.4:n.9829+34T>G
ENST00000680265.1:c.10051+34T>G	ENSP00000505384.1:n.10051+34T>G
ENST00000680710.1:c.9805+34T>G	ENSP00000506676.1:n.9805+34T>G
ENST00000294732.11:c.5074+34T>G	ENSP00000294732.7:n.5074+34T>G
ENST00000367408.5:c.2824+34T>G	ENSP00000356378.1:n.2824+34T>G
ENST00000367409.8:c.9829+34T>G	ENSP00000356379.4:n.9829+34T>G
ENST00000612785.1:c.3787+34T>G	ENSP00000479244.1:n.3787+34T>G
NM_001206846.1:c.5074+34T>G	NP_001193775.1:n.5074+34T>G
NM_018136.4:c.9829+34T>G	NP_060606.3:n.9829+34T>G
NM_018136.5:c.9829+34T>G MANE Select	NP_060606.3:n.9829+34T>G
NM_001206846.2:c.5074+34T>G	NP_001193775.1:n.5074+34T>G