Canonical Allele Identifier: CA2690915253

Gene: NANS TRIM14

Linked Data

• gnomAD v4: 9-98076756-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076757_98076758del , CM000671.2:g.98076757_98076758del	GRCh38
NC_000009.11:g.100839039_100839040del , CM000671.1:g.100839039_100839040del	GRCh37
NC_000009.10:g.99878860_99878861del	NCBI36
NG_052789.1:g.25081_25082del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.349-161_349-160del (NANS) MANE Select	ENSP00000210444.5:n.349-161_349-160del
ENST00000210444.5:c.349-161_349-160del (NANS)	ENSP00000210444.5:n.349-161_349-160del
ENST00000375098.7:c.*29-7071_*29-7070del (TRIM14)	ENSP00000364239.3:n.*29-7071_*29-7070del
ENST00000461452.1:n.2115_2116del (NANS)
ENST00000495319.1:n.553-161_553-160del (NANS)
NM_018946.3:c.349-161_349-160del (NANS)	NP_061819.2:n.349-161_349-160del
XM_011518787.1:c.1-161_1-160del (NANS)	XP_011517089.1:n.1-161_1-160del
XM_011518787.2:c.1-161_1-160del (NANS)	XP_011517089.1:n.1-161_1-160del
XM_017014811.1:c.-206-161_-206-160del (NANS)	XP_016870300.1:n.-206-161_-206-160del
XM_017015352.2:c.*29-4592_*29-4591del (TRIM14)	XP_016870841.1:n.*29-4592_*29-4591del
XM_024447574.1:c.-161_-160del (NANS)	XP_024303342.1:n.-161_-160del
NM_018946.4:c.349-161_349-160del (NANS) MANE Select	NP_061819.2:n.349-161_349-160del