Canonical Allele Identifier: CA422672487

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060154T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091024T>C , CM000663.2:g.197091024T>C	GRCh38
NC_000001.10:g.197060154T>C , CM000663.1:g.197060154T>C	GRCh37
NC_000001.9:g.195326777T>C	NCBI36
NG_015867.1:g.60671A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2749A>G
ENST00000367409.9:c.9462A>G MANE Select	ENSP00000356379.4:p.Arg3154=
ENST00000680265.1:c.9684A>G	ENSP00000505384.1:p.Arg3228=
ENST00000680710.1:c.9438A>G	ENSP00000506676.1:p.Arg3146=
ENST00000294732.11:c.4707A>G	ENSP00000294732.7:p.Arg1569=
ENST00000367408.5:c.2457A>G	ENSP00000356378.1:p.Arg819=
ENST00000367409.8:c.9462A>G	ENSP00000356379.4:p.Arg3154=
ENST00000612785.1:c.3420A>G	ENSP00000479244.1:p.Arg1140=
NM_001206846.1:c.4707A>G	NP_001193775.1:p.Arg1569=
NM_018136.4:c.9462A>G	NP_060606.3:p.Arg3154=
NM_018136.5:c.9462A>G MANE Select	NP_060606.3:p.Arg3154=
NM_001206846.2:c.4707A>G	NP_001193775.1:p.Arg1569=