Canonical Allele Identifier: CA343998357

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197057497C>G (hg19) ; chr1:g.197088367C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088367C>G , CM000663.2:g.197088367C>G	GRCh38
NC_000001.10:g.197057497C>G , CM000663.1:g.197057497C>G	GRCh37
NC_000001.9:g.195324120C>G	NCBI36
NG_015867.1:g.63328G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3337G>C
ENST00000367409.9:c.10050G>C MANE Select	ENSP00000356379.4:p.Leu3350Phe
ENST00000680265.1:c.10272G>C	ENSP00000505384.1:p.Leu3424Phe
ENST00000680710.1:c.10026G>C	ENSP00000506676.1:p.Leu3342Phe
ENST00000294732.11:c.5295G>C	ENSP00000294732.7:p.Leu1765Phe
ENST00000367408.5:c.3045G>C	ENSP00000356378.1:p.Leu1015Phe
ENST00000367409.8:c.10050G>C	ENSP00000356379.4:p.Leu3350Phe
ENST00000612785.1:c.4008G>C	ENSP00000479244.1:p.Leu1336Phe
NM_001206846.1:c.5295G>C	NP_001193775.1:p.Leu1765Phe
NM_018136.4:c.10050G>C	NP_060606.3:p.Leu3350Phe
NM_018136.5:c.10050G>C MANE Select	NP_060606.3:p.Leu3350Phe
NM_001206846.2:c.5295G>C	NP_001193775.1:p.Leu1765Phe