Canonical Allele Identifier: CA167066892

Gene: NUP205

Linked Data

• dbSNP Id: rs566444542
• gnomAD v3: 7-135645175-T-C
• gnomAD v4: 7-135645175-T-C
• MyVariant Identifiers: chr7:g.135329923T>C (hg19) ; chr7:g.135645175T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.135645175T>C , CM000669.2:g.135645175T>C	GRCh38
NC_000007.13:g.135329923T>C , CM000669.1:g.135329923T>C	GRCh37
NC_000007.12:g.134980463T>C	NCBI36
NG_051184.1:g.92262T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000285968.11:c.5683+157T>C MANE Select	ENSP00000285968.6:n.5683+157T>C
ENST00000285968.10:c.5683+157T>C	ENSP00000285968.6:n.5683+157T>C
ENST00000461255.5:n.890+157T>C
ENST00000477620.5:c.1405+197T>C
ENST00000490439.1:c.120+157T>C
ENST00000607647.5:n.3961+157T>C
NM_015135.2:c.5683+157T>C	NP_055950.1:n.5683+157T>C
XM_005250235.2:c.4609+157T>C	XP_005250292.1:n.4609+157T>C
NM_001329434.1:c.4609+157T>C	NP_001316363.1:n.4609+157T>C
NM_015135.3:c.5683+157T>C MANE Select	NP_055950.2:n.5683+157T>C
NM_001329434.2:c.4609+157T>C	NP_001316363.2:n.4609+157T>C