Canonical Allele Identifier: CA344039582
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs750399442

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197122244A>G , CM000663.2:g.197122244A>G GRCh38
NC_000001.10:g.197091374A>G , CM000663.1:g.197091374A>G GRCh37
NC_000001.9:g.195357997A>G NCBI36
NG_015867.1:g.29451T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.1698T>C
ENST00000367409.9:c.3656T>C MANE Select ENSP00000356379.4:p.Leu1219Ser
ENST00000680112.1:n.1712T>C
ENST00000680265.1:c.3656T>C ENSP00000505384.1:p.Leu1219Ser
ENST00000680710.1:c.3656T>C ENSP00000506676.1:p.Leu1219Ser
ENST00000681879.1:c.3656T>C ENSP00000505363.1:p.Leu1219Ser
ENST00000294732.11:c.3656T>C ENSP00000294732.7:p.Leu1219Ser
ENST00000367408.5:c.1406T>C ENSP00000356378.1:p.Leu469Ser
ENST00000367409.8:c.3656T>C ENSP00000356379.4:p.Leu1219Ser
ENST00000612785.1:c.562-19597T>C ENSP00000479244.1:n.562-19597T>C
NM_001206846.1:c.3656T>C NP_001193775.1:p.Leu1219Ser
NM_018136.4:c.3656T>C NP_060606.3:p.Leu1219Ser
NM_018136.5:c.3656T>C MANE Select NP_060606.3:p.Leu1219Ser
NM_001206846.2:c.3656T>C NP_001193775.1:p.Leu1219Ser