Canonical Allele Identifier: CA422672459

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060085A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090955A>G , CM000663.2:g.197090955A>G	GRCh38
NC_000001.10:g.197060085A>G , CM000663.1:g.197060085A>G	GRCh37
NC_000001.9:g.195326708A>G	NCBI36
NG_015867.1:g.60740T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2818T>C
ENST00000367409.9:c.9531T>C MANE Select	ENSP00000356379.4:p.Cys3177=
ENST00000680265.1:c.9753T>C	ENSP00000505384.1:p.Cys3251=
ENST00000680710.1:c.9507T>C	ENSP00000506676.1:p.Cys3169=
ENST00000294732.11:c.4776T>C	ENSP00000294732.7:p.Cys1592=
ENST00000367408.5:c.2526T>C	ENSP00000356378.1:p.Cys842=
ENST00000367409.8:c.9531T>C	ENSP00000356379.4:p.Cys3177=
ENST00000612785.1:c.3489T>C	ENSP00000479244.1:p.Cys1163=
NM_001206846.1:c.4776T>C	NP_001193775.1:p.Cys1592=
NM_018136.4:c.9531T>C	NP_060606.3:p.Cys3177=
NM_018136.5:c.9531T>C MANE Select	NP_060606.3:p.Cys3177=
NM_001206846.2:c.4776T>C	NP_001193775.1:p.Cys1592=