Canonical Allele Identifier: CA343997849

Gene: ASPM

Linked Data - Variant Effect Evidence

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197088321C>G , CM000663.2:g.197088321C>G	GRCh38
NC_000001.10:g.197057451C>G , CM000663.1:g.197057451C>G	GRCh37
NC_000001.9:g.195324074C>G	NCBI36
NG_015867.1:g.63374G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.3383G>C
ENST00000367409.9:c.10096G>C MANE Select	ENSP00000356379.4:p.Gly3366Arg
ENST00000680265.1:c.10318G>C	ENSP00000505384.1:p.Gly3440Arg
ENST00000680710.1:c.10072G>C	ENSP00000506676.1:p.Gly3358Arg
ENST00000294732.11:c.5341G>C	ENSP00000294732.7:p.Gly1781Arg
ENST00000367408.5:c.3091G>C	ENSP00000356378.1:p.Gly1031Arg
ENST00000367409.8:c.10096G>C	ENSP00000356379.4:p.Gly3366Arg
ENST00000612785.1:c.4054G>C	ENSP00000479244.1:p.Gly1352Arg
NM_001206846.1:c.5341G>C	NP_001193775.1:p.Gly1781Arg
NM_018136.4:c.10096G>C	NP_060606.3:p.Gly3366Arg
NM_018136.5:c.10096G>C MANE Select	NP_060606.3:p.Gly3366Arg
NM_001206846.2:c.5341G>C	NP_001193775.1:p.Gly1781Arg