Canonical Allele Identifier: CA343998739

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057549G>C (hg19) ; chr1:g.197088419G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088419G>C , CM000663.2:g.197088419G>C	GRCh38
NC_000001.10:g.197057549G>C , CM000663.1:g.197057549G>C	GRCh37
NC_000001.9:g.195324172G>C	NCBI36
NG_015867.1:g.63276C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3285C>G
ENST00000367409.9:c.9998C>G MANE Select	ENSP00000356379.4:p.Thr3333Ser
ENST00000680265.1:c.10220C>G	ENSP00000505384.1:p.Thr3407Ser
ENST00000680710.1:c.9974C>G	ENSP00000506676.1:p.Thr3325Ser
ENST00000294732.11:c.5243C>G	ENSP00000294732.7:p.Thr1748Ser
ENST00000367408.5:c.2993C>G	ENSP00000356378.1:p.Thr998Ser
ENST00000367409.8:c.9998C>G	ENSP00000356379.4:p.Thr3333Ser
ENST00000612785.1:c.3956C>G	ENSP00000479244.1:p.Thr1319Ser
NM_001206846.1:c.5243C>G	NP_001193775.1:p.Thr1748Ser
NM_018136.4:c.9998C>G	NP_060606.3:p.Thr3333Ser
NM_018136.5:c.9998C>G MANE Select	NP_060606.3:p.Thr3333Ser
NM_001206846.2:c.5243C>G	NP_001193775.1:p.Thr1748Ser