Canonical Allele Identifier: CA1143787569

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197122178T= , CM000663.2:g.197122178T=	GRCh38
NC_000001.10:g.197091308T= , CM000663.1:g.197091308T=	GRCh37
NC_000001.9:g.195357931T=	NCBI36
NG_015867.1:g.29517A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367408.6:n.1764A=
ENST00000367409.9:c.3722A= MANE Select	ENSP00000356379.4:p.Asn1241=
ENST00000680112.1:n.1778A=
ENST00000680265.1:c.3722A=	ENSP00000505384.1:p.Asn1241=
ENST00000680710.1:c.3722A=	ENSP00000506676.1:p.Asn1241=
ENST00000681879.1:c.3722A=	ENSP00000505363.1:p.Asn1241=
ENST00000294732.11:c.3722A=	ENSP00000294732.7:p.Asn1241=
ENST00000367408.5:c.1472A=	ENSP00000356378.1:p.Asn491=
ENST00000367409.8:c.3722A=	ENSP00000356379.4:p.Asn1241=
ENST00000612785.1:c.562-19531A=	ENSP00000479244.1:n.562-19531A=
NM_001206846.1:c.3722A=	NP_001193775.1:p.Asn1241=
NM_018136.4:c.3722A=	NP_060606.3:p.Asn1241=
NM_018136.5:c.3722A= MANE Select	NP_060606.3:p.Asn1241=
NM_001206846.2:c.3722A=	NP_001193775.1:p.Asn1241=