Canonical Allele Identifier: CA344040355

Gene: ASPM

Linked Data

• gnomAD v4: 1-197122507-G-A
• MyVariant Identifiers: chr1:g.197091637G>A (hg19) ; chr1:g.197122507G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197122507G>A , CM000663.2:g.197122507G>A	GRCh38
NC_000001.10:g.197091637G>A , CM000663.1:g.197091637G>A	GRCh37
NC_000001.9:g.195358260G>A	NCBI36
NG_015867.1:g.29188C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.1521C>T
ENST00000367409.9:c.3479C>T MANE Select	ENSP00000356379.4:p.Ala1160Val
ENST00000680112.1:n.1535C>T
ENST00000680265.1:c.3479C>T	ENSP00000505384.1:p.Ala1160Val
ENST00000680710.1:c.3479C>T	ENSP00000506676.1:p.Ala1160Val
ENST00000681879.1:c.3479C>T	ENSP00000505363.1:p.Ala1160Val
ENST00000294732.11:c.3479C>T	ENSP00000294732.7:p.Ala1160Val
ENST00000367408.5:c.1229C>T	ENSP00000356378.1:p.Ala410Val
ENST00000367409.8:c.3479C>T	ENSP00000356379.4:p.Ala1160Val
ENST00000612785.1:c.562-19860C>T	ENSP00000479244.1:n.562-19860C>T
NM_001206846.1:c.3479C>T	NP_001193775.1:p.Ala1160Val
NM_018136.4:c.3479C>T	NP_060606.3:p.Ala1160Val
NM_018136.5:c.3479C>T MANE Select	NP_060606.3:p.Ala1160Val
NM_001206846.2:c.3479C>T	NP_001193775.1:p.Ala1160Val