Canonical Allele Identifier: CA1149111403

Gene: ASPM

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.197122515T= , CM000663.2:g.197122515T=	GRCh38
NC_000001.10:g.197091645T= , CM000663.1:g.197091645T=	GRCh37
NC_000001.9:g.195358268T=	NCBI36
NG_015867.1:g.29180A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000367408.6:n.1513A=
ENST00000367409.9:c.3471A= MANE Select	ENSP00000356379.4:p.Pro1157=
ENST00000680112.1:n.1527A=
ENST00000680265.1:c.3471A=	ENSP00000505384.1:p.Pro1157=
ENST00000680710.1:c.3471A=	ENSP00000506676.1:p.Pro1157=
ENST00000681879.1:c.3471A=	ENSP00000505363.1:p.Pro1157=
ENST00000294732.11:c.3471A=	ENSP00000294732.7:p.Pro1157=
ENST00000367408.5:c.1221A=	ENSP00000356378.1:p.Pro407=
ENST00000367409.8:c.3471A=	ENSP00000356379.4:p.Pro1157=
ENST00000612785.1:c.562-19868A=	ENSP00000479244.1:n.562-19868A=
NM_001206846.1:c.3471A=	NP_001193775.1:p.Pro1157=
NM_018136.4:c.3471A=	NP_060606.3:p.Pro1157=
NM_018136.5:c.3471A= MANE Select	NP_060606.3:p.Pro1157=
NM_001206846.2:c.3471A=	NP_001193775.1:p.Pro1157=