Canonical Allele Identifier: CA1907224585

Gene: NCOA4

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.46027267T= , CM000672.2:g.46027267T=	GRCh38
NC_000010.10:g.51568555A= , CM000672.1:g.51568555A=	GRCh37
NC_000010.9:g.51238561A=	NCBI36
NG_023372.1:g.8448A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000581486.6:c.-15+3259A= MANE Select	ENSP00000462943.1:n.-15+3259A=
ENST00000578454.5:c.34+165A=	ENSP00000463027.1:n.34+165A=
ENST00000579039.2:c.34+165A=	ENSP00000463455.1:n.34+165A=
ENST00000580070.5:c.-128+3259A=	ENSP00000462352.1:n.-128+3259A=
ENST00000581486.5:c.-15+3259A=	ENSP00000462943.1:n.-15+3259A=
ENST00000585056.5:c.-71+3259A=	ENSP00000463022.1:n.-71+3259A=
NM_001145260.1:c.34+165A=	NP_001138732.1:n.34+165A=
NM_001145261.1:c.34+165A=	NP_001138733.1:n.34+165A=
NM_001145263.1:c.-15+3259A=	NP_001138735.1:n.-15+3259A=
NM_001145260.2:c.34+165A=	NP_001138732.1:n.34+165A=
NM_001145261.2:c.34+165A=	NP_001138733.1:n.34+165A=
NM_001145263.2:c.-15+3259A= MANE Select	NP_001138735.1:n.-15+3259A=