Canonical Allele Identifier: CA2690915457

Gene: NANS TRIM14

Linked Data

• gnomAD v4: 9-98077151-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98077151T>C , CM000671.2:g.98077151T>C	GRCh38
NC_000009.11:g.100839433T>C , CM000671.1:g.100839433T>C	GRCh37
NC_000009.10:g.99879254T>C	NCBI36
NG_052789.1:g.25475T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.448+134T>C (NANS) MANE Select	ENSP00000210444.5:n.448+134T>C
ENST00000210444.5:c.448+134T>C (NANS)	ENSP00000210444.5:n.448+134T>C
ENST00000375098.7:c.*29-7464A>G (TRIM14)	ENSP00000364239.3:n.*29-7464A>G
ENST00000415280.1:c.-107+134T>C (NANS)	ENSP00000404107.1:n.-107+134T>C
ENST00000461452.1:n.2375+134T>C (NANS)
ENST00000495319.1:n.652+134T>C (NANS)
NM_018946.3:c.448+134T>C (NANS)	NP_061819.2:n.448+134T>C
XM_011518787.1:c.100+134T>C (NANS)	XP_011517089.1:n.100+134T>C
XM_011518788.1:c.71+135T>C (NANS)	XP_011517090.1:n.71+135T>C
XM_011518787.2:c.100+134T>C (NANS)	XP_011517089.1:n.100+134T>C
XM_011518788.2:c.71+135T>C (NANS)	XP_011517090.1:n.71+135T>C
XM_017014811.1:c.-107+134T>C (NANS)	XP_016870300.1:n.-107+134T>C
XM_017015352.2:c.*29-4985A>G (TRIM14)	XP_016870841.1:n.*29-4985A>G
XM_024447574.1:c.100+134T>C (NANS)	XP_024303342.1:n.100+134T>C
NM_018946.4:c.448+134T>C (NANS) MANE Select	NP_061819.2:n.448+134T>C