Canonical Allele Identifier: CA344003473

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060133A>C (hg19) ; chr1:g.197091003A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091003A>C , CM000663.2:g.197091003A>C	GRCh38
NC_000001.10:g.197060133A>C , CM000663.1:g.197060133A>C	GRCh37
NC_000001.9:g.195326756A>C	NCBI36
NG_015867.1:g.60692T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2770T>G
ENST00000367409.9:c.9483T>G MANE Select	ENSP00000356379.4:p.Ile3161Met
ENST00000680265.1:c.9705T>G	ENSP00000505384.1:p.Ile3235Met
ENST00000680710.1:c.9459T>G	ENSP00000506676.1:p.Ile3153Met
ENST00000294732.11:c.4728T>G	ENSP00000294732.7:p.Ile1576Met
ENST00000367408.5:c.2478T>G	ENSP00000356378.1:p.Ile826Met
ENST00000367409.8:c.9483T>G	ENSP00000356379.4:p.Ile3161Met
ENST00000612785.1:c.3441T>G	ENSP00000479244.1:p.Ile1147Met
NM_001206846.1:c.4728T>G	NP_001193775.1:p.Ile1576Met
NM_018136.4:c.9483T>G	NP_060606.3:p.Ile3161Met
NM_018136.5:c.9483T>G MANE Select	NP_060606.3:p.Ile3161Met
NM_001206846.2:c.4728T>G	NP_001193775.1:p.Ile1576Met