Canonical Allele Identifier: CA343998564

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057520T>A (hg19) ; chr1:g.197088390T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088390T>A , CM000663.2:g.197088390T>A	GRCh38
NC_000001.10:g.197057520T>A , CM000663.1:g.197057520T>A	GRCh37
NC_000001.9:g.195324143T>A	NCBI36
NG_015867.1:g.63305A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3314A>T
ENST00000367409.9:c.10027A>T MANE Select	ENSP00000356379.4:p.Ile3343Leu
ENST00000680265.1:c.10249A>T	ENSP00000505384.1:p.Ile3417Leu
ENST00000680710.1:c.10003A>T	ENSP00000506676.1:p.Ile3335Leu
ENST00000294732.11:c.5272A>T	ENSP00000294732.7:p.Ile1758Leu
ENST00000367408.5:c.3022A>T	ENSP00000356378.1:p.Ile1008Leu
ENST00000367409.8:c.10027A>T	ENSP00000356379.4:p.Ile3343Leu
ENST00000612785.1:c.3985A>T	ENSP00000479244.1:p.Ile1329Leu
NM_001206846.1:c.5272A>T	NP_001193775.1:p.Ile1758Leu
NM_018136.4:c.10027A>T	NP_060606.3:p.Ile3343Leu
NM_018136.5:c.10027A>T MANE Select	NP_060606.3:p.Ile3343Leu
NM_001206846.2:c.5272A>T	NP_001193775.1:p.Ile1758Leu