Canonical Allele Identifier: CA422805187

Gene: ASPM

Linked Data

• gnomAD v4: 1-197090233-C-T
• MyVariant Identifiers: chr1:g.197059363C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090233C>T , CM000663.2:g.197090233C>T	GRCh38
NC_000001.10:g.197059363C>T , CM000663.1:g.197059363C>T	GRCh37
NC_000001.9:g.195325986C>T	NCBI36
NG_015867.1:g.61462G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3079G>A
ENST00000367409.9:c.9792G>A MANE Select	ENSP00000356379.4:p.Lys3264=
ENST00000680265.1:c.10014G>A	ENSP00000505384.1:p.Lys3338=
ENST00000680710.1:c.9768G>A	ENSP00000506676.1:p.Lys3256=
ENST00000294732.11:c.5037G>A	ENSP00000294732.7:p.Lys1679=
ENST00000367408.5:c.2787G>A	ENSP00000356378.1:p.Lys929=
ENST00000367409.8:c.9792G>A	ENSP00000356379.4:p.Lys3264=
ENST00000612785.1:c.3750G>A	ENSP00000479244.1:p.Lys1250=
NM_001206846.1:c.5037G>A	NP_001193775.1:p.Lys1679=
NM_018136.4:c.9792G>A	NP_060606.3:p.Lys3264=
NM_018136.5:c.9792G>A MANE Select	NP_060606.3:p.Lys3264=
NM_001206846.2:c.5037G>A	NP_001193775.1:p.Lys1679=