Canonical Allele Identifier: CA1143355825

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197122505_197122510delinsTAGCGT , CM000663.2:g.197122505_197122510delinsTAGCGT	GRCh38
NC_000001.10:g.197091635_197091640delinsTAGCGT , CM000663.1:g.197091635_197091640delinsTAGCGT	GRCh37
NC_000001.9:g.195358258_195358263delinsTAGCGT	NCBI36
NG_015867.1:g.29185_29190delinsACGCTA

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.1518_1523delinsACGCTA
ENST00000367409.9:c.3476_3481delinsACGCTA MANE Select	ENSP00000356379.4:p.Asp1159=
ENST00000680112.1:n.1532_1537delinsACGCTA
ENST00000680265.1:c.3476_3481delinsACGCTA	ENSP00000505384.1:p.Asp1159=
ENST00000680710.1:c.3476_3481delinsACGCTA	ENSP00000506676.1:p.Asp1159=
ENST00000681879.1:c.3476_3481delinsACGCTA	ENSP00000505363.1:p.Asp1159=
ENST00000294732.11:c.3476_3481delinsACGCTA	ENSP00000294732.7:p.Asp1159=
ENST00000367408.5:c.1226_1231delinsACGCTA	ENSP00000356378.1:p.Asp409=
ENST00000367409.8:c.3476_3481delinsACGCTA	ENSP00000356379.4:p.Asp1159=
ENST00000612785.1:c.562-19863_562-19858delinsACGCTA	ENSP00000479244.1:n.562-19863_562-19858de...
NM_001206846.1:c.3476_3481delinsACGCTA	NP_001193775.1:p.Asp1159=
NM_018136.4:c.3476_3481delinsACGCTA	NP_060606.3:p.Asp1159=
NM_018136.5:c.3476_3481delinsACGCTA MANE Select	NP_060606.3:p.Asp1159=
NM_001206846.2:c.3476_3481delinsACGCTA	NP_001193775.1:p.Asp1159=