Canonical Allele Identifier: CA528535181

Gene: ASPM

Linked Data

• dbSNP Id: rs772828137
• gnomAD v2: 1-197086907-A-C
• gnomAD v4: 1-197117777-A-C
• MyVariant Identifiers: chr1:g.197086907A>C (hg19) ; chr1:g.197117777A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197117777A>C , CM000663.2:g.197117777A>C	GRCh38
NC_000001.10:g.197086907A>C , CM000663.1:g.197086907A>C	GRCh37
NC_000001.9:g.195353530A>C	NCBI36
NG_015867.1:g.33918T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2107+12T>G
ENST00000367409.9:c.4065+12T>G MANE Select	ENSP00000356379.4:n.4065+12T>G
ENST00000680265.1:c.4065+12T>G	ENSP00000505384.1:n.4065+12T>G
ENST00000680710.1:c.4065+12T>G	ENSP00000506676.1:n.4065+12T>G
ENST00000681879.1:c.4113+12T>G	ENSP00000505363.1:n.4113+12T>G
ENST00000294732.11:c.4065+12T>G	ENSP00000294732.7:n.4065+12T>G
ENST00000367408.5:c.1815+12T>G	ENSP00000356378.1:n.1815+12T>G
ENST00000367409.8:c.4065+12T>G	ENSP00000356379.4:n.4065+12T>G
ENST00000612785.1:c.562-15130T>G	ENSP00000479244.1:n.562-15130T>G
NM_001206846.1:c.4065+12T>G	NP_001193775.1:n.4065+12T>G
NM_018136.4:c.4065+12T>G	NP_060606.3:n.4065+12T>G
NM_018136.5:c.4065+12T>G MANE Select	NP_060606.3:n.4065+12T>G
NM_001206846.2:c.4065+12T>G	NP_001193775.1:n.4065+12T>G