Canonical Allele Identifier: CA344036079

Gene: ASPM

Linked Data

• dbSNP Id: rs1421096456
• gnomAD v2: 1-197086923-A-G
• gnomAD v4: 1-197117793-A-G
• MyVariant Identifiers: chr1:g.197086923A>G (hg19) ; chr1:g.197117793A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197117793A>G , CM000663.2:g.197117793A>G	GRCh38
NC_000001.10:g.197086923A>G , CM000663.1:g.197086923A>G	GRCh37
NC_000001.9:g.195353546A>G	NCBI36
NG_015867.1:g.33902T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2103T>C
ENST00000367409.9:c.4061T>C MANE Select	ENSP00000356379.4:p.Ile1354Thr
ENST00000680265.1:c.4061T>C	ENSP00000505384.1:p.Ile1354Thr
ENST00000680710.1:c.4061T>C	ENSP00000506676.1:p.Ile1354Thr
ENST00000681879.1:c.4109T>C	ENSP00000505363.1:n.4109T>C
ENST00000294732.11:c.4061T>C	ENSP00000294732.7:p.Ile1354Thr
ENST00000367408.5:c.1811T>C	ENSP00000356378.1:p.Ile604Thr
ENST00000367409.8:c.4061T>C	ENSP00000356379.4:p.Ile1354Thr
ENST00000612785.1:c.562-15146T>C	ENSP00000479244.1:n.562-15146T>C
NM_001206846.1:c.4061T>C	NP_001193775.1:p.Ile1354Thr
NM_018136.4:c.4061T>C	NP_060606.3:p.Ile1354Thr
NM_018136.5:c.4061T>C MANE Select	NP_060606.3:p.Ile1354Thr
NM_001206846.2:c.4061T>C	NP_001193775.1:p.Ile1354Thr