Canonical Allele Identifier: CA2690915345

Gene: NANS TRIM14

Linked Data

• gnomAD v4: 9-98076892-AGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076893_98076894del , CM000671.2:g.98076893_98076894del	GRCh38
NC_000009.11:g.100839175_100839176del , CM000671.1:g.100839175_100839176del	GRCh37
NC_000009.10:g.99878996_99878997del	NCBI36
NG_052789.1:g.25217_25218del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.349-25_349-24del (NANS) MANE Select	ENSP00000210444.5:n.349-25_349-24del
ENST00000210444.5:c.349-25_349-24del (NANS)	ENSP00000210444.5:n.349-25_349-24del
ENST00000375098.7:c.*29-7207_*29-7206del (TRIM14)	ENSP00000364239.3:n.*29-7207_*29-7206del
ENST00000415280.1:c.-231_-230del (NANS)	ENSP00000404107.1:n.-231_-230del
ENST00000461452.1:n.2251_2252del (NANS)
ENST00000495319.1:n.553-25_553-24del (NANS)
NM_018946.3:c.349-25_349-24del (NANS)	NP_061819.2:n.349-25_349-24del
XM_011518787.1:c.1-25_1-24del (NANS)	XP_011517089.1:n.1-25_1-24del
XM_011518787.2:c.1-25_1-24del (NANS)	XP_011517089.1:n.1-25_1-24del
XM_017014811.1:c.-206-25_-206-24del (NANS)	XP_016870300.1:n.-206-25_-206-24del
XM_017015352.2:c.*29-4728_*29-4727del (TRIM14)	XP_016870841.1:n.*29-4728_*29-4727del
XM_024447574.1:c.-25_-24del (NANS)	XP_024303342.1:n.-25_-24del
NM_018946.4:c.349-25_349-24del (NANS) MANE Select	NP_061819.2:n.349-25_349-24del