Canonical Allele Identifier: CA344039395
Gene: ASPM HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197122214C>A , CM000663.2:g.197122214C>A GRCh38
NC_000001.10:g.197091344C>A , CM000663.1:g.197091344C>A GRCh37
NC_000001.9:g.195357967C>A NCBI36
NG_015867.1:g.29481G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.1728G>T
ENST00000367409.9:c.3686G>T MANE Select ENSP00000356379.4:p.Gly1229Val
ENST00000680112.1:n.1742G>T
ENST00000680265.1:c.3686G>T ENSP00000505384.1:p.Gly1229Val
ENST00000680710.1:c.3686G>T ENSP00000506676.1:p.Gly1229Val
ENST00000681879.1:c.3686G>T ENSP00000505363.1:p.Gly1229Val
ENST00000294732.11:c.3686G>T ENSP00000294732.7:p.Gly1229Val
ENST00000367408.5:c.1436G>T ENSP00000356378.1:p.Gly479Val
ENST00000367409.8:c.3686G>T ENSP00000356379.4:p.Gly1229Val
ENST00000612785.1:c.562-19567G>T ENSP00000479244.1:n.562-19567G>T
NM_001206846.1:c.3686G>T NP_001193775.1:p.Gly1229Val
NM_018136.4:c.3686G>T NP_060606.3:p.Gly1229Val
NM_018136.5:c.3686G>T MANE Select NP_060606.3:p.Gly1229Val
NM_001206846.2:c.3686G>T NP_001193775.1:p.Gly1229Val