Canonical Allele Identifier: CA2649660606

Gene: ASPM

Linked Data

• gnomAD v4: 1-197090101-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090101_197090102insT , CM000663.2:g.197090101_197090102insT	GRCh38
NC_000001.10:g.197059231_197059232insT , CM000663.1:g.197059231_197059232insT	GRCh37
NC_000001.9:g.195325854_195325855insT	NCBI36
NG_015867.1:g.61593_61594insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3117-18_3117-17insA
ENST00000367409.9:c.9830-18_9830-17insA MANE Select	ENSP00000356379.4:n.9830-18_9830-17insA
ENST00000680265.1:c.10052-18_10052-17insA	ENSP00000505384.1:n.10052-18_10052-17insA
ENST00000680710.1:c.9806-18_9806-17insA	ENSP00000506676.1:n.9806-18_9806-17insA
ENST00000294732.11:c.5075-18_5075-17insA	ENSP00000294732.7:n.5075-18_5075-17insA
ENST00000367408.5:c.2825-18_2825-17insA	ENSP00000356378.1:n.2825-18_2825-17insA
ENST00000367409.8:c.9830-18_9830-17insA	ENSP00000356379.4:n.9830-18_9830-17insA
ENST00000612785.1:c.3788-18_3788-17insA	ENSP00000479244.1:n.3788-18_3788-17insA
NM_001206846.1:c.5075-18_5075-17insA	NP_001193775.1:n.5075-18_5075-17insA
NM_018136.4:c.9830-18_9830-17insA	NP_060606.3:n.9830-18_9830-17insA
NM_018136.5:c.9830-18_9830-17insA MANE Select	NP_060606.3:n.9830-18_9830-17insA
NM_001206846.2:c.5075-18_5075-17insA	NP_001193775.1:n.5075-18_5075-17insA