Canonical Allele Identifier: CA832638623

Gene: UNCX

Linked Data

• dbSNP Id: rs1453943751
• MyVariant Identifiers: chr7:g.1273906_1273907insG (hg19) ; chr7:g.1234270_1234271insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234271dup , CM000669.2:g.1234271dup	GRCh38
NC_000007.13:g.1273907dup , CM000669.1:g.1273907dup	GRCh37
NC_000007.12:g.1240433dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+576dup MANE Select	ENSP00000314480.8:n.450+576dup
ENST00000316333.8:c.450+576dup	ENSP00000314480.8:n.450+576dup
NM_001080461.1:c.450+576dup	NP_001073930.1:n.450+576dup
NM_001080461.2:c.450+576dup	NP_001073930.1:n.450+576dup
NM_001080461.3:c.450+576dup MANE Select	NP_001073930.1:n.450+576dup