Canonical Allele Identifier: CA466419771

Gene: NANS TRIM14

Linked Data

• MyVariant Identifiers: chr9:g.100839253T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076971T>C , CM000671.2:g.98076971T>C	GRCh38
NC_000009.11:g.100839253T>C , CM000671.1:g.100839253T>C	GRCh37
NC_000009.10:g.99879074T>C	NCBI36
NG_052789.1:g.25295T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.402T>C (NANS) MANE Select	ENSP00000210444.5:p.Ser134=
ENST00000210444.5:c.402T>C (NANS)	ENSP00000210444.5:p.Ser134=
ENST00000375098.7:c.*29-7284A>G (TRIM14)	ENSP00000364239.3:n.*29-7284A>G
ENST00000415280.1:c.-153T>C (NANS)	ENSP00000404107.1:n.-153T>C
ENST00000461452.1:n.2329T>C (NANS)
ENST00000495319.1:n.606T>C (NANS)
NM_018946.3:c.402T>C (NANS)	NP_061819.2:p.Ser134=
XM_011518787.1:c.54T>C (NANS)	XP_011517089.1:p.Ser18=
XM_011518788.1:c.26T>C (NANS)	XP_011517090.1:p.Leu9Pro
XM_011518787.2:c.54T>C (NANS)	XP_011517089.1:p.Ser18=
XM_011518788.2:c.26T>C (NANS)	XP_011517090.1:p.Leu9Pro
XM_017014811.1:c.-153T>C (NANS)	XP_016870300.1:n.-153T>C
XM_017015352.2:c.*29-4805A>G (TRIM14)	XP_016870841.1:n.*29-4805A>G
XM_024447574.1:c.54T>C (NANS)	XP_024303342.1:p.Ser18=
NM_018946.4:c.402T>C (NANS) MANE Select	NP_061819.2:p.Ser134=