Canonical Allele Identifier: CA344018600

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197112498T>G (hg19) ; chr1:g.197143368T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197143368T>G , CM000663.2:g.197143368T>G	GRCh38
NC_000001.10:g.197112498T>G , CM000663.1:g.197112498T>G	GRCh37
NC_000001.9:g.195379121T>G	NCBI36
NG_015867.1:g.8327A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367409.9:c.884A>C MANE Select	ENSP00000356379.4:p.Lys295Thr
ENST00000679766.1:n.1101A>C
ENST00000680265.1:c.884A>C	ENSP00000505384.1:p.Lys295Thr
ENST00000680710.1:c.884A>C	ENSP00000506676.1:p.Lys295Thr
ENST00000681879.1:c.884A>C	ENSP00000505363.1:p.Lys295Thr
ENST00000294732.11:c.884A>C	ENSP00000294732.7:p.Lys295Thr
ENST00000367409.8:c.884A>C	ENSP00000356379.4:p.Lys295Thr
ENST00000612785.1:c.561+323A>C	ENSP00000479244.1:n.561+323A>C
NM_001206846.1:c.884A>C	NP_001193775.1:p.Lys295Thr
NM_018136.4:c.884A>C	NP_060606.3:p.Lys295Thr
NM_018136.5:c.884A>C MANE Select	NP_060606.3:p.Lys295Thr
NM_001206846.2:c.884A>C	NP_001193775.1:p.Lys295Thr