Canonical Allele Identifier: CA152421557

Gene: UNCX

Linked Data

• dbSNP Id: rs145576795
• MyVariant Identifiers: chr7:g.1273702del (hg19) ; chr7:g.1234066del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.1234066del , CM000669.2:g.1234066del	GRCh38
NC_000007.13:g.1273702del , CM000669.1:g.1273702del	GRCh37
NC_000007.12:g.1240228del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000316333.9:c.450+371del MANE Select	ENSP00000314480.8:n.450+371del
ENST00000316333.8:c.450+371del	ENSP00000314480.8:n.450+371del
NM_001080461.1:c.450+371del	NP_001073930.1:n.450+371del
NM_001080461.2:c.450+371del	NP_001073930.1:n.450+371del
NM_001080461.3:c.450+371del MANE Select	NP_001073930.1:n.450+371del