Canonical Allele Identifier: CA2649662298

Gene: ASPM

Linked Data

• gnomAD v4: 1-197123984-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197123984A>G , CM000663.2:g.197123984A>G	GRCh38
NC_000001.10:g.197093114A>G , CM000663.1:g.197093114A>G	GRCh37
NC_000001.9:g.195359737A>G	NCBI36
NG_015867.1:g.27711T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.1432+126T>C
ENST00000367409.9:c.3390+126T>C MANE Select	ENSP00000356379.4:n.3390+126T>C
ENST00000680112.1:n.1446+126T>C
ENST00000680265.1:c.3390+126T>C	ENSP00000505384.1:n.3390+126T>C
ENST00000680710.1:c.3390+126T>C	ENSP00000506676.1:n.3390+126T>C
ENST00000681879.1:c.3390+126T>C	ENSP00000505363.1:n.3390+126T>C
ENST00000294732.11:c.3390+126T>C	ENSP00000294732.7:n.3390+126T>C
ENST00000367408.5:c.1140+126T>C	ENSP00000356378.1:n.1140+126T>C
ENST00000367409.8:c.3390+126T>C	ENSP00000356379.4:n.3390+126T>C
ENST00000612785.1:c.561+19707T>C	ENSP00000479244.1:n.561+19707T>C
NM_001206846.1:c.3390+126T>C	NP_001193775.1:n.3390+126T>C
NM_018136.4:c.3390+126T>C	NP_060606.3:n.3390+126T>C
NM_018136.5:c.3390+126T>C MANE Select	NP_060606.3:n.3390+126T>C
NM_001206846.2:c.3390+126T>C	NP_001193775.1:n.3390+126T>C