Canonical Allele Identifier: CA344001706

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059371T>C (hg19) ; chr1:g.197090241T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090241T>C , CM000663.2:g.197090241T>C	GRCh38
NC_000001.10:g.197059371T>C , CM000663.1:g.197059371T>C	GRCh37
NC_000001.9:g.195325994T>C	NCBI36
NG_015867.1:g.61454A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3071A>G
ENST00000367409.9:c.9784A>G MANE Select	ENSP00000356379.4:p.Thr3262Ala
ENST00000680265.1:c.10006A>G	ENSP00000505384.1:p.Thr3336Ala
ENST00000680710.1:c.9760A>G	ENSP00000506676.1:p.Thr3254Ala
ENST00000294732.11:c.5029A>G	ENSP00000294732.7:p.Thr1677Ala
ENST00000367408.5:c.2779A>G	ENSP00000356378.1:p.Thr927Ala
ENST00000367409.8:c.9784A>G	ENSP00000356379.4:p.Thr3262Ala
ENST00000612785.1:c.3742A>G	ENSP00000479244.1:p.Thr1248Ala
NM_001206846.1:c.5029A>G	NP_001193775.1:p.Thr1677Ala
NM_018136.4:c.9784A>G	NP_060606.3:p.Thr3262Ala
NM_018136.5:c.9784A>G MANE Select	NP_060606.3:p.Thr3262Ala
NM_001206846.2:c.5029A>G	NP_001193775.1:p.Thr1677Ala