Canonical Allele Identifier: CA1682451559

Gene: UNCX

Linked Data

• dbSNP Id: rs751327990

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234079_1234085dup , CM000669.2:g.1234079_1234085dup	GRCh38
NC_000007.13:g.1273715_1273721dup , CM000669.1:g.1273715_1273721dup	GRCh37
NC_000007.12:g.1240241_1240247dup	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+384_450+390dup MANE Select	ENSP00000314480.8:n.450+384_450+390dup
ENST00000316333.8:c.450+384_450+390dup	ENSP00000314480.8:n.450+384_450+390dup
NM_001080461.1:c.450+384_450+390dup	NP_001073930.1:n.450+384_450+390dup
NM_001080461.2:c.450+384_450+390dup	NP_001073930.1:n.450+384_450+390dup
NM_001080461.3:c.450+384_450+390dup MANE Select	NP_001073930.1:n.450+384_450+390dup