Canonical Allele Identifier: CA1143355921

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197101059_197101061delinsTCT , CM000663.2:g.197101059_197101061delinsTCT	GRCh38
NC_000001.10:g.197070189_197070191delinsTCT , CM000663.1:g.197070189_197070191delinsTCT	GRCh37
NC_000001.9:g.195336812_195336814delinsTCT	NCBI36
NG_015867.1:g.50634_50636delinsAGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2108-4897_2108-4895delinsAGA
ENST00000367409.9:c.8190_8192delinsAGA MANE Select	ENSP00000356379.4:p.Thr2730=
ENST00000680265.1:c.8190_8192delinsAGA	ENSP00000505384.1:p.Thr2730=
ENST00000680710.1:c.8190_8192delinsAGA	ENSP00000506676.1:p.Thr2730=
ENST00000294732.11:c.4066-4897_4066-4895delinsAGA	ENSP00000294732.7:n.4066-4897_4066-4895delinsAGA
ENST00000367408.5:c.1816-4897_1816-4895delinsAGA	ENSP00000356378.1:n.1816-4897_1816-4895delinsAGA
ENST00000367409.8:c.8190_8192delinsAGA	ENSP00000356379.4:p.Thr2730=
ENST00000612785.1:c.2148_2150delinsAGA	ENSP00000479244.1:p.Thr716=
NM_001206846.1:c.4066-4897_4066-4895delinsAGA	NP_001193775.1:n.4066-4897_4066-4895delinsAGA
NM_018136.4:c.8190_8192delinsAGA	NP_060606.3:p.Thr2730=
NM_018136.5:c.8190_8192delinsAGA MANE Select	NP_060606.3:p.Thr2730=
NM_001206846.2:c.4066-4897_4066-4895delinsAGA	NP_001193775.1:n.4066-4897_4066-4895delinsAGA