Canonical Allele Identifier: CA344003579

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060142C>G (hg19) ; chr1:g.197091012C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091012C>G , CM000663.2:g.197091012C>G	GRCh38
NC_000001.10:g.197060142C>G , CM000663.1:g.197060142C>G	GRCh37
NC_000001.9:g.195326765C>G	NCBI36
NG_015867.1:g.60683G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2761G>C
ENST00000367409.9:c.9474G>C MANE Select	ENSP00000356379.4:p.Lys3158Asn
ENST00000680265.1:c.9696G>C	ENSP00000505384.1:p.Lys3232Asn
ENST00000680710.1:c.9450G>C	ENSP00000506676.1:p.Lys3150Asn
ENST00000294732.11:c.4719G>C	ENSP00000294732.7:p.Lys1573Asn
ENST00000367408.5:c.2469G>C	ENSP00000356378.1:p.Lys823Asn
ENST00000367409.8:c.9474G>C	ENSP00000356379.4:p.Lys3158Asn
ENST00000612785.1:c.3432G>C	ENSP00000479244.1:p.Lys1144Asn
NM_001206846.1:c.4719G>C	NP_001193775.1:p.Lys1573Asn
NM_018136.4:c.9474G>C	NP_060606.3:p.Lys3158Asn
NM_018136.5:c.9474G>C MANE Select	NP_060606.3:p.Lys3158Asn
NM_001206846.2:c.4719G>C	NP_001193775.1:p.Lys1573Asn