Canonical Allele Identifier: CA466419702

Gene: NANS TRIM14

Linked Data

• MyVariant Identifiers: chr9:g.100839208T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076926T>A , CM000671.2:g.98076926T>A	GRCh38
NC_000009.11:g.100839208T>A , CM000671.1:g.100839208T>A	GRCh37
NC_000009.10:g.99879029T>A	NCBI36
NG_052789.1:g.25250T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.357T>A (NANS) MANE Select	ENSP00000210444.5:p.Val119=
ENST00000210444.5:c.357T>A (NANS)	ENSP00000210444.5:p.Val119=
ENST00000375098.7:c.*29-7239A>T (TRIM14)	ENSP00000364239.3:n.*29-7239A>T
ENST00000415280.1:c.-198T>A (NANS)	ENSP00000404107.1:n.-198T>A
ENST00000461452.1:n.2284T>A (NANS)
ENST00000495319.1:n.561T>A (NANS)
NM_018946.3:c.357T>A (NANS)	NP_061819.2:p.Val119=
XM_011518787.1:c.9T>A (NANS)	XP_011517089.1:p.Val3=
XM_011518787.2:c.9T>A (NANS)	XP_011517089.1:p.Val3=
XM_017014811.1:c.-198T>A (NANS)	XP_016870300.1:n.-198T>A
XM_017015352.2:c.*29-4760A>T (TRIM14)	XP_016870841.1:n.*29-4760A>T
XM_024447574.1:c.9T>A (NANS)	XP_024303342.1:p.Val3=
NM_018946.4:c.357T>A (NANS) MANE Select	NP_061819.2:p.Val119=