Canonical Allele Identifier: CA344003707

Gene: ASPM

Linked Data

• MyVariant Identifiers: chr1:g.197060159C>A (hg19) ; chr1:g.197091029C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197091029C>A , CM000663.2:g.197091029C>A	GRCh38
NC_000001.10:g.197060159C>A , CM000663.1:g.197060159C>A	GRCh37
NC_000001.9:g.195326782C>A	NCBI36
NG_015867.1:g.60666G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.2744G>T
ENST00000367409.9:c.9457G>T MANE Select	ENSP00000356379.4:p.Ala3153Ser
ENST00000680265.1:c.9679G>T	ENSP00000505384.1:p.Ala3227Ser
ENST00000680710.1:c.9433G>T	ENSP00000506676.1:p.Ala3145Ser
ENST00000294732.11:c.4702G>T	ENSP00000294732.7:p.Ala1568Ser
ENST00000367408.5:c.2452G>T	ENSP00000356378.1:p.Ala818Ser
ENST00000367409.8:c.9457G>T	ENSP00000356379.4:p.Ala3153Ser
ENST00000612785.1:c.3415G>T	ENSP00000479244.1:p.Ala1139Ser
NM_001206846.1:c.4702G>T	NP_001193775.1:p.Ala1568Ser
NM_018136.4:c.9457G>T	NP_060606.3:p.Ala3153Ser
NM_018136.5:c.9457G>T MANE Select	NP_060606.3:p.Ala3153Ser
NM_001206846.2:c.4702G>T	NP_001193775.1:p.Ala1568Ser