Canonical Allele Identifier: CA1217946508

Gene: ASPM

Linked Data

• dbSNP Id: rs1658607684
• gnomAD v4: 1-197142237-TATA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197142241_197142243del , CM000663.2:g.197142241_197142243del	GRCh38
NC_000001.10:g.197111371_197111373del , CM000663.1:g.197111371_197111373del	GRCh37
NC_000001.9:g.195377994_195377996del	NCBI36
NG_015867.1:g.9455_9457del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1921+91_1921+93del MANE Select	ENSP00000356379.4:n.1921+91_1921+93del
ENST00000679766.1:n.2138+91_2138+93del
ENST00000680265.1:c.1921+91_1921+93del	ENSP00000505384.1:n.1921+91_1921+93del
ENST00000680710.1:c.1921+91_1921+93del	ENSP00000506676.1:n.1921+91_1921+93del
ENST00000681879.1:c.1921+91_1921+93del	ENSP00000505363.1:n.1921+91_1921+93del
ENST00000294732.11:c.1921+91_1921+93del	ENSP00000294732.7:n.1921+91_1921+93del
ENST00000367409.8:c.1921+91_1921+93del	ENSP00000356379.4:n.1921+91_1921+93del
ENST00000612785.1:c.561+1451_561+1453del	ENSP00000479244.1:n.561+1451_561+1453del
NM_001206846.1:c.1921+91_1921+93del	NP_001193775.1:n.1921+91_1921+93del
NM_018136.4:c.1921+91_1921+93del	NP_060606.3:n.1921+91_1921+93del
NM_018136.5:c.1921+91_1921+93del MANE Select	NP_060606.3:n.1921+91_1921+93del
NM_001206846.2:c.1921+91_1921+93del	NP_001193775.1:n.1921+91_1921+93del