Canonical Allele Identifier: CA869034859

Gene: NANS TRIM14

Linked Data

• dbSNP Id: rs1457827472
• gnomAD v3: 9-98077129-TTTTCATTTTTTTAAA-T
• gnomAD v4: 9-98077129-TTTTCATTTTTTTAAA-T
• MyVariant Identifiers: chr9:g.100839412_100839426del (hg19) ; chr9:g.98077130_98077144del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98077131_98077145del , CM000671.2:g.98077131_98077145del	GRCh38
NC_000009.11:g.100839413_100839427del , CM000671.1:g.100839413_100839427del	GRCh37
NC_000009.10:g.99879234_99879248del	NCBI36
NG_052789.1:g.25455_25469del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.448+114_448+128del (NANS) MANE Select	ENSP00000210444.5:n.448+114_448+128del
ENST00000210444.5:c.448+114_448+128del (NANS)	ENSP00000210444.5:n.448+114_448+128del
ENST00000375098.7:c.*29-7457_*29-7443del (TRIM14)	ENSP00000364239.3:n.*29-7457_*29-7443del
ENST00000415280.1:c.-107+114_-107+128del (NANS)	ENSP00000404107.1:n.-107+114_-107+128del
ENST00000461452.1:n.2375+114_2375+128del (NANS)
ENST00000495319.1:n.652+114_652+128del (NANS)
NM_018946.3:c.448+114_448+128del (NANS)	NP_061819.2:n.448+114_448+128del
XM_011518787.1:c.100+114_100+128del (NANS)	XP_011517089.1:n.100+114_100+128del
XM_011518788.1:c.71+115_71+129del (NANS)	XP_011517090.1:n.71+115_71+129del
XM_011518787.2:c.100+114_100+128del (NANS)	XP_011517089.1:n.100+114_100+128del
XM_011518788.2:c.71+115_71+129del (NANS)	XP_011517090.1:n.71+115_71+129del
XM_017014811.1:c.-107+114_-107+128del (NANS)	XP_016870300.1:n.-107+114_-107+128del
XM_017015352.2:c.*29-4978_*29-4964del (TRIM14)	XP_016870841.1:n.*29-4978_*29-4964del
XM_024447574.1:c.100+114_100+128del (NANS)	XP_024303342.1:n.100+114_100+128del
NM_018946.4:c.448+114_448+128del (NANS) MANE Select	NP_061819.2:n.448+114_448+128del