Canonical Allele Identifier: CA344048509

Gene: ASPM

Linked Data

• dbSNP Id: rs1658160310
• COSMIC: COSM6005828
• MyVariant Identifiers: chr1:g.197097672C>A (hg19) ; chr1:g.197128542C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197128542C>A , CM000663.2:g.197128542C>A	GRCh38
NC_000001.10:g.197097672C>A , CM000663.1:g.197097672C>A	GRCh37
NC_000001.9:g.195364295C>A	NCBI36
NG_015867.1:g.23153G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.836G>T
ENST00000367409.9:c.2884G>T MANE Select	ENSP00000356379.4:p.Asp962Tyr
ENST00000680112.1:n.940G>T
ENST00000680265.1:c.2884G>T	ENSP00000505384.1:p.Asp962Tyr
ENST00000680710.1:c.2884G>T	ENSP00000506676.1:p.Asp962Tyr
ENST00000681879.1:c.2884G>T	ENSP00000505363.1:p.Asp962Tyr
ENST00000294732.11:c.2884G>T	ENSP00000294732.7:p.Asp962Tyr
ENST00000367408.5:c.634G>T	ENSP00000356378.1:p.Asp212Tyr
ENST00000367409.8:c.2884G>T	ENSP00000356379.4:p.Asp962Tyr
ENST00000612785.1:c.561+15149G>T	ENSP00000479244.1:n.561+15149G>T
NM_001206846.1:c.2884G>T	NP_001193775.1:p.Asp962Tyr
NM_018136.4:c.2884G>T	NP_060606.3:p.Asp962Tyr
NM_018136.5:c.2884G>T MANE Select	NP_060606.3:p.Asp962Tyr
NM_001206846.2:c.2884G>T	NP_001193775.1:p.Asp962Tyr