Canonical Allele Identifier: CA466419734

Gene: NANS TRIM14

Linked Data

• MyVariant Identifiers: chr9:g.100839229T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076947T>C , CM000671.2:g.98076947T>C	GRCh38
NC_000009.11:g.100839229T>C , CM000671.1:g.100839229T>C	GRCh37
NC_000009.10:g.99879050T>C	NCBI36
NG_052789.1:g.25271T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.378T>C (NANS) MANE Select	ENSP00000210444.5:p.Asn126=
ENST00000210444.5:c.378T>C (NANS)	ENSP00000210444.5:p.Asn126=
ENST00000375098.7:c.*29-7260A>G (TRIM14)	ENSP00000364239.3:n.*29-7260A>G
ENST00000415280.1:c.-177T>C (NANS)	ENSP00000404107.1:n.-177T>C
ENST00000461452.1:n.2305T>C (NANS)
ENST00000495319.1:n.582T>C (NANS)
NM_018946.3:c.378T>C (NANS)	NP_061819.2:p.Asn126=
XM_011518787.1:c.30T>C (NANS)	XP_011517089.1:p.Asn10=
XM_011518788.1:c.2T>C (NANS)	XP_011517090.1:p.Met1Thr
XM_011518787.2:c.30T>C (NANS)	XP_011517089.1:p.Asn10=
XM_011518788.2:c.2T>C (NANS)	XP_011517090.1:p.Met1Thr
XM_017014811.1:c.-177T>C (NANS)	XP_016870300.1:n.-177T>C
XM_017015352.2:c.*29-4781A>G (TRIM14)	XP_016870841.1:n.*29-4781A>G
XM_024447574.1:c.30T>C (NANS)	XP_024303342.1:p.Asn10=
NM_018946.4:c.378T>C (NANS) MANE Select	NP_061819.2:p.Asn126=