Canonical Allele Identifier: CA422673149

Gene: ASPM

Linked Data

• gnomAD v4: 1-197093175-C-T
• MyVariant Identifiers: chr1:g.197062305C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093175C>T , CM000663.2:g.197093175C>T	GRCh38
NC_000001.10:g.197062305C>T , CM000663.1:g.197062305C>T	GRCh37
NC_000001.9:g.195328928C>T	NCBI36
NG_015867.1:g.58520G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2458G>A
ENST00000367409.9:c.9171G>A MANE Select	ENSP00000356379.4:p.Leu3057=
ENST00000680265.1:c.9393G>A	ENSP00000505384.1:p.Leu3131=
ENST00000680710.1:c.9171G>A	ENSP00000506676.1:p.Leu3057=
ENST00000294732.11:c.4416G>A	ENSP00000294732.7:p.Leu1472=
ENST00000367408.5:c.2166G>A	ENSP00000356378.1:p.Leu722=
ENST00000367409.8:c.9171G>A	ENSP00000356379.4:p.Leu3057=
ENST00000612785.1:c.3129G>A	ENSP00000479244.1:p.Leu1043=
NM_001206846.1:c.4416G>A	NP_001193775.1:p.Leu1472=
NM_018136.4:c.9171G>A	NP_060606.3:p.Leu3057=
NM_018136.5:c.9171G>A MANE Select	NP_060606.3:p.Leu3057=
NM_001206846.2:c.4416G>A	NP_001193775.1:p.Leu1472=