Canonical Allele Identifier: CA343998634

Gene: ASPM

Linked Data

• gnomAD v4: 1-197088401-A-G
• MyVariant Identifiers: chr1:g.197057531A>G (hg19) ; chr1:g.197088401A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088401A>G , CM000663.2:g.197088401A>G	GRCh38
NC_000001.10:g.197057531A>G , CM000663.1:g.197057531A>G	GRCh37
NC_000001.9:g.195324154A>G	NCBI36
NG_015867.1:g.63294T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3303T>C
ENST00000367409.9:c.10016T>C MANE Select	ENSP00000356379.4:p.Val3339Ala
ENST00000680265.1:c.10238T>C	ENSP00000505384.1:p.Val3413Ala
ENST00000680710.1:c.9992T>C	ENSP00000506676.1:p.Val3331Ala
ENST00000294732.11:c.5261T>C	ENSP00000294732.7:p.Val1754Ala
ENST00000367408.5:c.3011T>C	ENSP00000356378.1:p.Val1004Ala
ENST00000367409.8:c.10016T>C	ENSP00000356379.4:p.Val3339Ala
ENST00000612785.1:c.3974T>C	ENSP00000479244.1:p.Val1325Ala
NM_001206846.1:c.5261T>C	NP_001193775.1:p.Val1754Ala
NM_018136.4:c.10016T>C	NP_060606.3:p.Val3339Ala
NM_018136.5:c.10016T>C MANE Select	NP_060606.3:p.Val3339Ala
NM_001206846.2:c.5261T>C	NP_001193775.1:p.Val1754Ala