Canonical Allele Identifier: CA374197631

Gene: NANS TRIM14

Linked Data

• MyVariant Identifiers: chr9:g.100839254G>T (hg19) ; chr9:g.98076972G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076972G>T , CM000671.2:g.98076972G>T	GRCh38
NC_000009.11:g.100839254G>T , CM000671.1:g.100839254G>T	GRCh37
NC_000009.10:g.99879075G>T	NCBI36
NG_052789.1:g.25296G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.403G>T (NANS) MANE Select	ENSP00000210444.5:p.Gly135Ter
ENST00000210444.5:c.403G>T (NANS)	ENSP00000210444.5:p.Gly135Ter
ENST00000375098.7:c.*29-7285C>A (TRIM14)	ENSP00000364239.3:n.*29-7285C>A
ENST00000415280.1:c.-152G>T (NANS)	ENSP00000404107.1:n.-152G>T
ENST00000461452.1:n.2330G>T (NANS)
ENST00000495319.1:n.607G>T (NANS)
NM_018946.3:c.403G>T (NANS)	NP_061819.2:p.Gly135Ter
XM_011518787.1:c.55G>T (NANS)	XP_011517089.1:p.Gly19Ter
XM_011518788.1:c.27G>T (NANS)	XP_011517090.1:p.Leu9=
XM_011518787.2:c.55G>T (NANS)	XP_011517089.1:p.Gly19Ter
XM_011518788.2:c.27G>T (NANS)	XP_011517090.1:p.Leu9=
XM_017014811.1:c.-152G>T (NANS)	XP_016870300.1:n.-152G>T
XM_017015352.2:c.*29-4806C>A (TRIM14)	XP_016870841.1:n.*29-4806C>A
XM_024447574.1:c.55G>T (NANS)	XP_024303342.1:p.Gly19Ter
NM_018946.4:c.403G>T (NANS) MANE Select	NP_061819.2:p.Gly135Ter