Canonical Allele Identifier: CA344001692

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197059365T>A (hg19) ; chr1:g.197090235T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197090235T>A , CM000663.2:g.197090235T>A	GRCh38
NC_000001.10:g.197059365T>A , CM000663.1:g.197059365T>A	GRCh37
NC_000001.9:g.195325988T>A	NCBI36
NG_015867.1:g.61460A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.3077A>T
ENST00000367409.9:c.9790A>T MANE Select	ENSP00000356379.4:p.Lys3264Ter
ENST00000680265.1:c.10012A>T	ENSP00000505384.1:p.Lys3338Ter
ENST00000680710.1:c.9766A>T	ENSP00000506676.1:p.Lys3256Ter
ENST00000294732.11:c.5035A>T	ENSP00000294732.7:p.Lys1679Ter
ENST00000367408.5:c.2785A>T	ENSP00000356378.1:p.Lys929Ter
ENST00000367409.8:c.9790A>T	ENSP00000356379.4:p.Lys3264Ter
ENST00000612785.1:c.3748A>T	ENSP00000479244.1:p.Lys1250Ter
NM_001206846.1:c.5035A>T	NP_001193775.1:p.Lys1679Ter
NM_018136.4:c.9790A>T	NP_060606.3:p.Lys3264Ter
NM_018136.5:c.9790A>T MANE Select	NP_060606.3:p.Lys3264Ter
NM_001206846.2:c.5035A>T	NP_001193775.1:p.Lys1679Ter