Canonical Allele Identifier: CA1143355924

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197101390_197101392delinsTCT , CM000663.2:g.197101390_197101392delinsTCT	GRCh38
NC_000001.10:g.197070520_197070522delinsTCT , CM000663.1:g.197070520_197070522delinsTCT	GRCh37
NC_000001.9:g.195337143_195337145delinsTCT	NCBI36
NG_015867.1:g.50303_50305delinsAGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2108-5228_2108-5226delinsAGA
ENST00000367409.9:c.7859_7861delinsAGA MANE Select	ENSP00000356379.4:p.Gln2620=
ENST00000680265.1:c.7859_7861delinsAGA	ENSP00000505384.1:p.Gln2620=
ENST00000680710.1:c.7859_7861delinsAGA	ENSP00000506676.1:p.Gln2620=
ENST00000294732.11:c.4066-5228_4066-5226delinsAGA	ENSP00000294732.7:n.4066-5228_4066-5226de...
ENST00000367408.5:c.1816-5228_1816-5226delinsAGA	ENSP00000356378.1:n.1816-5228_1816-5226de...
ENST00000367409.8:c.7859_7861delinsAGA	ENSP00000356379.4:p.Gln2620=
ENST00000612785.1:c.1817_1819delinsAGA	ENSP00000479244.1:p.Gln606=
NM_001206846.1:c.4066-5228_4066-5226delinsAGA	NP_001193775.1:n.4066-5228_4066-5226delin...
NM_018136.4:c.7859_7861delinsAGA	NP_060606.3:p.Gln2620=
NM_018136.5:c.7859_7861delinsAGA MANE Select	NP_060606.3:p.Gln2620=
NM_001206846.2:c.4066-5228_4066-5226delinsAGA	NP_001193775.1:n.4066-5228_4066-5226delin...