Canonical Allele Identifier: CA343998288

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057490A>C (hg19) ; chr1:g.197088360A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088360A>C , CM000663.2:g.197088360A>C	GRCh38
NC_000001.10:g.197057490A>C , CM000663.1:g.197057490A>C	GRCh37
NC_000001.9:g.195324113A>C	NCBI36
NG_015867.1:g.63335T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3344T>G
ENST00000367409.9:c.10057T>G MANE Select	ENSP00000356379.4:p.Tyr3353Asp
ENST00000680265.1:c.10279T>G	ENSP00000505384.1:p.Tyr3427Asp
ENST00000680710.1:c.10033T>G	ENSP00000506676.1:p.Tyr3345Asp
ENST00000294732.11:c.5302T>G	ENSP00000294732.7:p.Tyr1768Asp
ENST00000367408.5:c.3052T>G	ENSP00000356378.1:p.Tyr1018Asp
ENST00000367409.8:c.10057T>G	ENSP00000356379.4:p.Tyr3353Asp
ENST00000612785.1:c.4015T>G	ENSP00000479244.1:p.Tyr1339Asp
NM_001206846.1:c.5302T>G	NP_001193775.1:p.Tyr1768Asp
NM_018136.4:c.10057T>G	NP_060606.3:p.Tyr3353Asp
NM_018136.5:c.10057T>G MANE Select	NP_060606.3:p.Tyr3353Asp
NM_001206846.2:c.5302T>G	NP_001193775.1:p.Tyr1768Asp