Canonical Allele Identifier: CA1682451732

Gene: UNCX

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234357A= , CM000669.2:g.1234357A=	GRCh38
NC_000007.13:g.1273993A= , CM000669.1:g.1273993A=	GRCh37
NC_000007.12:g.1240519A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+662A= MANE Select	ENSP00000314480.8:n.450+662A=
ENST00000316333.8:c.450+662A=	ENSP00000314480.8:n.450+662A=
NM_001080461.1:c.450+662A=	NP_001073930.1:n.450+662A=
NM_001080461.2:c.450+662A=	NP_001073930.1:n.450+662A=
NM_001080461.3:c.450+662A= MANE Select	NP_001073930.1:n.450+662A=