Canonical Allele Identifier: CA374197257

Gene: NANS TRIM14

Linked Data

• MyVariant Identifiers: chr9:g.100839206G>A (hg19) ; chr9:g.98076924G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076924G>A , CM000671.2:g.98076924G>A	GRCh38
NC_000009.11:g.100839206G>A , CM000671.1:g.100839206G>A	GRCh37
NC_000009.10:g.99879027G>A	NCBI36
NG_052789.1:g.25248G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.355G>A (NANS) MANE Select	ENSP00000210444.5:p.Val119Ile
ENST00000210444.5:c.355G>A (NANS)	ENSP00000210444.5:p.Val119Ile
ENST00000375098.7:c.*29-7237C>T (TRIM14)	ENSP00000364239.3:n.*29-7237C>T
ENST00000415280.1:c.-200G>A (NANS)	ENSP00000404107.1:n.-200G>A
ENST00000461452.1:n.2282G>A (NANS)
ENST00000495319.1:n.559G>A (NANS)
NM_018946.3:c.355G>A (NANS)	NP_061819.2:p.Val119Ile
XM_011518787.1:c.7G>A (NANS)	XP_011517089.1:p.Val3Ile
XM_011518787.2:c.7G>A (NANS)	XP_011517089.1:p.Val3Ile
XM_017014811.1:c.-200G>A (NANS)	XP_016870300.1:n.-200G>A
XM_017015352.2:c.*29-4758C>T (TRIM14)	XP_016870841.1:n.*29-4758C>T
XM_024447574.1:c.7G>A (NANS)	XP_024303342.1:p.Val3Ile
NM_018946.4:c.355G>A (NANS) MANE Select	NP_061819.2:p.Val119Ile