Canonical Allele Identifier: CA344002896

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060078G>A (hg19) ; chr1:g.197090948G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090948G>A , CM000663.2:g.197090948G>A	GRCh38
NC_000001.10:g.197060078G>A , CM000663.1:g.197060078G>A	GRCh37
NC_000001.9:g.195326701G>A	NCBI36
NG_015867.1:g.60747C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.2825C>T
ENST00000367409.9:c.9538C>T MANE Select	ENSP00000356379.4:p.Gln3180Ter
ENST00000680265.1:c.9760C>T	ENSP00000505384.1:p.Gln3254Ter
ENST00000680710.1:c.9514C>T	ENSP00000506676.1:p.Gln3172Ter
ENST00000294732.11:c.4783C>T	ENSP00000294732.7:p.Gln1595Ter
ENST00000367408.5:c.2533C>T	ENSP00000356378.1:p.Gln845Ter
ENST00000367409.8:c.9538C>T	ENSP00000356379.4:p.Gln3180Ter
ENST00000612785.1:c.3496C>T	ENSP00000479244.1:p.Gln1166Ter
NM_001206846.1:c.4783C>T	NP_001193775.1:p.Gln1595Ter
NM_018136.4:c.9538C>T	NP_060606.3:p.Gln3180Ter
NM_018136.5:c.9538C>T MANE Select	NP_060606.3:p.Gln3180Ter
NM_001206846.2:c.4783C>T	NP_001193775.1:p.Gln1595Ter