Canonical Allele Identifier: CA344042088

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197093335C>G (hg19) ; chr1:g.197124205C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197124205C>G , CM000663.2:g.197124205C>G	GRCh38
NC_000001.10:g.197093335C>G , CM000663.1:g.197093335C>G	GRCh37
NC_000001.9:g.195359958C>G	NCBI36
NG_015867.1:g.27490G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.1337G>C
ENST00000367409.9:c.3295G>C MANE Select	ENSP00000356379.4:p.Gly1099Arg
ENST00000680112.1:n.1351G>C
ENST00000680265.1:c.3295G>C	ENSP00000505384.1:p.Gly1099Arg
ENST00000680710.1:c.3295G>C	ENSP00000506676.1:p.Gly1099Arg
ENST00000681879.1:c.3295G>C	ENSP00000505363.1:p.Gly1099Arg
ENST00000294732.11:c.3295G>C	ENSP00000294732.7:p.Gly1099Arg
ENST00000367408.5:c.1045G>C	ENSP00000356378.1:p.Gly349Arg
ENST00000367409.8:c.3295G>C	ENSP00000356379.4:p.Gly1099Arg
ENST00000612785.1:c.561+19486G>C	ENSP00000479244.1:n.561+19486G>C
NM_001206846.1:c.3295G>C	NP_001193775.1:p.Gly1099Arg
NM_018136.4:c.3295G>C	NP_060606.3:p.Gly1099Arg
NM_018136.5:c.3295G>C MANE Select	NP_060606.3:p.Gly1099Arg
NM_001206846.2:c.3295G>C	NP_001193775.1:p.Gly1099Arg