Canonical Allele Identifier: CA344007722

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197062365T>G (hg19) ; chr1:g.197093235T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093235T>G , CM000663.2:g.197093235T>G	GRCh38
NC_000001.10:g.197062365T>G , CM000663.1:g.197062365T>G	GRCh37
NC_000001.9:g.195328988T>G	NCBI36
NG_015867.1:g.58460A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2398A>C
ENST00000367409.9:c.9111A>C MANE Select	ENSP00000356379.4:p.Gln3037His
ENST00000680265.1:c.9333A>C	ENSP00000505384.1:p.Gln3111His
ENST00000680710.1:c.9111A>C	ENSP00000506676.1:p.Gln3037His
ENST00000294732.11:c.4356A>C	ENSP00000294732.7:p.Gln1452His
ENST00000367408.5:c.2106A>C	ENSP00000356378.1:p.Gln702His
ENST00000367409.8:c.9111A>C	ENSP00000356379.4:p.Gln3037His
ENST00000612785.1:c.3069A>C	ENSP00000479244.1:p.Gln1023His
NM_001206846.1:c.4356A>C	NP_001193775.1:p.Gln1452His
NM_018136.4:c.9111A>C	NP_060606.3:p.Gln3037His
NM_018136.5:c.9111A>C MANE Select	NP_060606.3:p.Gln3037His
NM_001206846.2:c.4356A>C	NP_001193775.1:p.Gln1452His