Canonical Allele Identifier: CA1217936779
Gene: ASPM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.197139747T= , CM000663.2:g.197139747T= GRCh38
NC_000001.10:g.197108877T= , CM000663.1:g.197108877T= GRCh37
NC_000001.9:g.195375500T= NCBI36
NG_015867.1:g.11948A=

Transcript Alleles

HGVS Amino-acid change
ENST00000367409.9:c.2026+20A= MANE Select ENSP00000356379.4:n.2026+20A=
ENST00000679766.1:n.2263A=
ENST00000680112.1:n.82+20A=
ENST00000680265.1:c.2026+20A= ENSP00000505384.1:n.2026+20A=
ENST00000680710.1:c.2026+20A= ENSP00000506676.1:n.2026+20A=
ENST00000681879.1:c.2026+20A= ENSP00000505363.1:n.2026+20A=
ENST00000294732.11:c.2026+20A= ENSP00000294732.7:n.2026+20A=
ENST00000367409.8:c.2026+20A= ENSP00000356379.4:n.2026+20A=
ENST00000612785.1:c.561+3944A= ENSP00000479244.1:n.561+3944A=
NM_001206846.1:c.2026+20A= NP_001193775.1:n.2026+20A=
NM_018136.4:c.2026+20A= NP_060606.3:n.2026+20A=
NM_018136.5:c.2026+20A= MANE Select NP_060606.3:n.2026+20A=
NM_001206846.2:c.2026+20A= NP_001193775.1:n.2026+20A=