Canonical Allele Identifier: CA1309034
Gene: ASPM HGNC NCBI

Linked Data

dbSNP Id: rs376964056

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197093215T>G , CM000663.2:g.197093215T>G GRCh38
NC_000001.10:g.197062345T>G , CM000663.1:g.197062345T>G GRCh37
NC_000001.9:g.195328968T>G NCBI36
NG_015867.1:g.58480A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367408.6:n.2418A>C
ENST00000367409.9:c.9131A>C MANE Select ENSP00000356379.4:p.Lys3044Thr
ENST00000680265.1:c.9353A>C ENSP00000505384.1:p.Lys3118Thr
ENST00000680710.1:c.9131A>C ENSP00000506676.1:p.Lys3044Thr
ENST00000294732.11:c.4376A>C ENSP00000294732.7:p.Lys1459Thr
ENST00000367408.5:c.2126A>C ENSP00000356378.1:p.Lys709Thr
ENST00000367409.8:c.9131A>C ENSP00000356379.4:p.Lys3044Thr
ENST00000612785.1:c.3089A>C ENSP00000479244.1:p.Lys1030Thr
NM_001206846.1:c.4376A>C NP_001193775.1:p.Lys1459Thr
NM_018136.4:c.9131A>C NP_060606.3:p.Lys3044Thr
NM_018136.5:c.9131A>C MANE Select NP_060606.3:p.Lys3044Thr
NM_001206846.2:c.4376A>C NP_001193775.1:p.Lys1459Thr