Canonical Allele Identifier: CA343998776

Gene: ASPM

Linked Data

• dbSNP Id: rs1252361392
• gnomAD v2: 1-197057554-T-G
• gnomAD v4: 1-197088424-T-G
• MyVariant Identifiers: chr1:g.197057554T>G (hg19) ; chr1:g.197088424T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088424T>G , CM000663.2:g.197088424T>G	GRCh38
NC_000001.10:g.197057554T>G , CM000663.1:g.197057554T>G	GRCh37
NC_000001.9:g.195324177T>G	NCBI36
NG_015867.1:g.63271A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3280A>C
ENST00000367409.9:c.9993A>C MANE Select	ENSP00000356379.4:p.Lys3331Asn
ENST00000680265.1:c.10215A>C	ENSP00000505384.1:p.Lys3405Asn
ENST00000680710.1:c.9969A>C	ENSP00000506676.1:p.Lys3323Asn
ENST00000294732.11:c.5238A>C	ENSP00000294732.7:p.Lys1746Asn
ENST00000367408.5:c.2988A>C	ENSP00000356378.1:p.Lys996Asn
ENST00000367409.8:c.9993A>C	ENSP00000356379.4:p.Lys3331Asn
ENST00000612785.1:c.3951A>C	ENSP00000479244.1:p.Lys1317Asn
NM_001206846.1:c.5238A>C	NP_001193775.1:p.Lys1746Asn
NM_018136.4:c.9993A>C	NP_060606.3:p.Lys3331Asn
NM_018136.5:c.9993A>C MANE Select	NP_060606.3:p.Lys3331Asn
NM_001206846.2:c.5238A>C	NP_001193775.1:p.Lys1746Asn