Canonical Allele Identifier: CA1148224829

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197122046_197122053delinsAAAAAAAA , CM000663.2:g.197122046_197122053delinsAAAAAAAA	GRCh38
NC_000001.10:g.197091176_197091183delinsAAAAAAAA , CM000663.1:g.197091176_197091183delinsAAAAAAAA	GRCh37
NC_000001.9:g.195357799_195357806delinsAAAAAAAA	NCBI36
NG_015867.1:g.29642_29649delinsTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.1784-10_1784-3delinsTTTTTTTT
ENST00000367409.9:c.3742-10_3742-3delinsTTTTTTTT MANE Select	ENSP00000356379.4:n.3742-10_3742-3delinsTTTTTTTT
ENST00000680112.1:n.1798-10_1798-3delinsTTTTTTTT
ENST00000680265.1:c.3742-10_3742-3delinsTTTTTTTT	ENSP00000505384.1:n.3742-10_3742-3delinsTTTTTTTT
ENST00000680710.1:c.3742-10_3742-3delinsTTTTTTTT	ENSP00000506676.1:n.3742-10_3742-3delinsTTTTTTTT
ENST00000681879.1:c.3742-10_3742-3delinsTTTTTTTT	ENSP00000505363.1:n.3742-10_3742-3delinsTTTTTTTT
ENST00000294732.11:c.3742-10_3742-3delinsTTTTTTTT	ENSP00000294732.7:n.3742-10_3742-3delinsTTTTTTTT
ENST00000367408.5:c.1492-10_1492-3delinsTTTTTTTT	ENSP00000356378.1:n.1492-10_1492-3delinsTTTTTTTT
ENST00000367409.8:c.3742-10_3742-3delinsTTTTTTTT	ENSP00000356379.4:n.3742-10_3742-3delinsTTTTTTTT
ENST00000612785.1:c.562-19406_562-19399delinsTTTTTTTT	ENSP00000479244.1:n.562-19406_562-19399delinsTTTTTTTT
NM_001206846.1:c.3742-10_3742-3delinsTTTTTTTT	NP_001193775.1:n.3742-10_3742-3delinsTTTTTTTT
NM_018136.4:c.3742-10_3742-3delinsTTTTTTTT	NP_060606.3:n.3742-10_3742-3delinsTTTTTTTT
NM_018136.5:c.3742-10_3742-3delinsTTTTTTTT MANE Select	NP_060606.3:n.3742-10_3742-3delinsTTTTTTTT
NM_001206846.2:c.3742-10_3742-3delinsTTTTTTTT	NP_001193775.1:n.3742-10_3742-3delinsTTTTTTTT