Canonical Allele Identifier: CA344017689

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197112306T>G (hg19) ; chr1:g.197143176T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197143176T>G , CM000663.2:g.197143176T>G	GRCh38
NC_000001.10:g.197112306T>G , CM000663.1:g.197112306T>G	GRCh37
NC_000001.9:g.195378929T>G	NCBI36
NG_015867.1:g.8519A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.1076A>C MANE Select	ENSP00000356379.4:p.His359Pro
ENST00000679766.1:n.1293A>C
ENST00000680265.1:c.1076A>C	ENSP00000505384.1:p.His359Pro
ENST00000680710.1:c.1076A>C	ENSP00000506676.1:p.His359Pro
ENST00000681879.1:c.1076A>C	ENSP00000505363.1:p.His359Pro
ENST00000294732.11:c.1076A>C	ENSP00000294732.7:p.His359Pro
ENST00000367409.8:c.1076A>C	ENSP00000356379.4:p.His359Pro
ENST00000612785.1:c.561+515A>C	ENSP00000479244.1:n.561+515A>C
NM_001206846.1:c.1076A>C	NP_001193775.1:p.His359Pro
NM_018136.4:c.1076A>C	NP_060606.3:p.His359Pro
NM_018136.5:c.1076A>C MANE Select	NP_060606.3:p.His359Pro
NM_001206846.2:c.1076A>C	NP_001193775.1:p.His359Pro