Canonical Allele Identifier: CA344007499

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197062335C>A (hg19) ; chr1:g.197093205C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197093205C>A , CM000663.2:g.197093205C>A	GRCh38
NC_000001.10:g.197062335C>A , CM000663.1:g.197062335C>A	GRCh37
NC_000001.9:g.195328958C>A	NCBI36
NG_015867.1:g.58490G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2428G>T
ENST00000367409.9:c.9141G>T MANE Select	ENSP00000356379.4:p.Gln3047His
ENST00000680265.1:c.9363G>T	ENSP00000505384.1:p.Gln3121His
ENST00000680710.1:c.9141G>T	ENSP00000506676.1:p.Gln3047His
ENST00000294732.11:c.4386G>T	ENSP00000294732.7:p.Gln1462His
ENST00000367408.5:c.2136G>T	ENSP00000356378.1:p.Gln712His
ENST00000367409.8:c.9141G>T	ENSP00000356379.4:p.Gln3047His
ENST00000612785.1:c.3099G>T	ENSP00000479244.1:p.Gln1033His
NM_001206846.1:c.4386G>T	NP_001193775.1:p.Gln1462His
NM_018136.4:c.9141G>T	NP_060606.3:p.Gln3047His
NM_018136.5:c.9141G>T MANE Select	NP_060606.3:p.Gln3047His
NM_001206846.2:c.4386G>T	NP_001193775.1:p.Gln1462His