Canonical Allele Identifier: CA422807937

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197091636A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197122506A>C , CM000663.2:g.197122506A>C	GRCh38
NC_000001.10:g.197091636A>C , CM000663.1:g.197091636A>C	GRCh37
NC_000001.9:g.195358259A>C	NCBI36
NG_015867.1:g.29189T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.1522T>G
ENST00000367409.9:c.3480T>G MANE Select	ENSP00000356379.4:p.Ala1160=
ENST00000680112.1:n.1536T>G
ENST00000680265.1:c.3480T>G	ENSP00000505384.1:p.Ala1160=
ENST00000680710.1:c.3480T>G	ENSP00000506676.1:p.Ala1160=
ENST00000681879.1:c.3480T>G	ENSP00000505363.1:p.Ala1160=
ENST00000294732.11:c.3480T>G	ENSP00000294732.7:p.Ala1160=
ENST00000367408.5:c.1230T>G	ENSP00000356378.1:p.Ala410=
ENST00000367409.8:c.3480T>G	ENSP00000356379.4:p.Ala1160=
ENST00000612785.1:c.562-19859T>G	ENSP00000479244.1:n.562-19859T>G
NM_001206846.1:c.3480T>G	NP_001193775.1:p.Ala1160=
NM_018136.4:c.3480T>G	NP_060606.3:p.Ala1160=
NM_018136.5:c.3480T>G MANE Select	NP_060606.3:p.Ala1160=
NM_001206846.2:c.3480T>G	NP_001193775.1:p.Ala1160=