Canonical Allele Identifier: CA344007035
Gene: ASPM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197093136C>A , CM000663.2:g.197093136C>A GRCh38
NC_000001.10:g.197062266C>A , CM000663.1:g.197062266C>A GRCh37
NC_000001.9:g.195328889C>A NCBI36
NG_015867.1:g.58559G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2497G>T
ENST00000367409.9:c.9210G>T MANE Select ENSP00000356379.4:p.Lys3070Asn
ENST00000680265.1:c.9432G>T ENSP00000505384.1:p.Lys3144Asn
ENST00000680710.1:c.9210G>T ENSP00000506676.1:p.Lys3070Asn
ENST00000294732.11:c.4455G>T ENSP00000294732.7:p.Lys1485Asn
ENST00000367408.5:c.2205G>T ENSP00000356378.1:p.Lys735Asn
ENST00000367409.8:c.9210G>T ENSP00000356379.4:p.Lys3070Asn
ENST00000612785.1:c.3168G>T ENSP00000479244.1:p.Lys1056Asn
NM_001206846.1:c.4455G>T NP_001193775.1:p.Lys1485Asn
NM_018136.4:c.9210G>T NP_060606.3:p.Lys3070Asn
NM_018136.5:c.9210G>T MANE Select NP_060606.3:p.Lys3070Asn
NM_001206846.2:c.4455G>T NP_001193775.1:p.Lys1485Asn