Canonical Allele Identifier: CA2690915341

Gene: NANS TRIM14

Linked Data

• gnomAD v4: 9-98076883-ATGGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076884_98076887del , CM000671.2:g.98076884_98076887del	GRCh38
NC_000009.11:g.100839166_100839169del , CM000671.1:g.100839166_100839169del	GRCh37
NC_000009.10:g.99878987_99878990del	NCBI36
NG_052789.1:g.25208_25211del

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.349-34_349-31del (NANS) MANE Select	ENSP00000210444.5:n.349-34_349-31del
ENST00000210444.5:c.349-34_349-31del (NANS)	ENSP00000210444.5:n.349-34_349-31del
ENST00000375098.7:c.*29-7200_*29-7197del (TRIM14)	ENSP00000364239.3:n.*29-7200_*29-7197del
ENST00000415280.1:c.-240_-237del (NANS)	ENSP00000404107.1:n.-240_-237del
ENST00000461452.1:n.2242_2245del (NANS)
ENST00000495319.1:n.553-34_553-31del (NANS)
NM_018946.3:c.349-34_349-31del (NANS)	NP_061819.2:n.349-34_349-31del
XM_011518787.1:c.1-34_1-31del (NANS)	XP_011517089.1:n.1-34_1-31del
XM_011518787.2:c.1-34_1-31del (NANS)	XP_011517089.1:n.1-34_1-31del
XM_017014811.1:c.-206-34_-206-31del (NANS)	XP_016870300.1:n.-206-34_-206-31del
XM_017015352.2:c.*29-4721_*29-4718del (TRIM14)	XP_016870841.1:n.*29-4721_*29-4718del
XM_024447574.1:c.-34_-31del (NANS)	XP_024303342.1:n.-34_-31del
NM_018946.4:c.349-34_349-31del (NANS) MANE Select	NP_061819.2:n.349-34_349-31del