Canonical Allele Identifier: CA1682451445

Gene: UNCX

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1233936T= , CM000669.2:g.1233936T=	GRCh38
NC_000007.13:g.1273572T= , CM000669.1:g.1273572T=	GRCh37
NC_000007.12:g.1240098T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316333.9:c.450+241T= MANE Select	ENSP00000314480.8:n.450+241T=
ENST00000316333.8:c.450+241T=	ENSP00000314480.8:n.450+241T=
NM_001080461.1:c.450+241T=	NP_001073930.1:n.450+241T=
NM_001080461.2:c.450+241T=	NP_001073930.1:n.450+241T=
NM_001080461.3:c.450+241T= MANE Select	NP_001073930.1:n.450+241T=