Canonical Allele Identifier: CA2690915266

Gene: NANS TRIM14

Linked Data

• gnomAD v4: 9-98076781-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076781G>T , CM000671.2:g.98076781G>T	GRCh38
NC_000009.11:g.100839063G>T , CM000671.1:g.100839063G>T	GRCh37
NC_000009.10:g.99878884G>T	NCBI36
NG_052789.1:g.25105G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.349-137G>T (NANS) MANE Select	ENSP00000210444.5:n.349-137G>T
ENST00000210444.5:c.349-137G>T (NANS)	ENSP00000210444.5:n.349-137G>T
ENST00000375098.7:c.*29-7094C>A (TRIM14)	ENSP00000364239.3:n.*29-7094C>A
ENST00000461452.1:n.2139G>T (NANS)
ENST00000495319.1:n.553-137G>T (NANS)
NM_018946.3:c.349-137G>T (NANS)	NP_061819.2:n.349-137G>T
XM_011518787.1:c.1-137G>T (NANS)	XP_011517089.1:n.1-137G>T
XM_011518787.2:c.1-137G>T (NANS)	XP_011517089.1:n.1-137G>T
XM_017014811.1:c.-206-137G>T (NANS)	XP_016870300.1:n.-206-137G>T
XM_017015352.2:c.*29-4615C>A (TRIM14)	XP_016870841.1:n.*29-4615C>A
XM_024447574.1:c.-137G>T (NANS)	XP_024303342.1:n.-137G>T
NM_018946.4:c.349-137G>T (NANS) MANE Select	NP_061819.2:n.349-137G>T