Canonical Allele Identifier: CA374197626

Gene: NANS TRIM14

Linked Data

• MyVariant Identifiers: chr9:g.100839251T>G (hg19) ; chr9:g.98076969T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076969T>G , CM000671.2:g.98076969T>G	GRCh38
NC_000009.11:g.100839251T>G , CM000671.1:g.100839251T>G	GRCh37
NC_000009.10:g.99879072T>G	NCBI36
NG_052789.1:g.25293T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.400T>G (NANS) MANE Select	ENSP00000210444.5:p.Ser134Ala
ENST00000210444.5:c.400T>G (NANS)	ENSP00000210444.5:p.Ser134Ala
ENST00000375098.7:c.*29-7282A>C (TRIM14)	ENSP00000364239.3:n.*29-7282A>C
ENST00000415280.1:c.-155T>G (NANS)	ENSP00000404107.1:n.-155T>G
ENST00000461452.1:n.2327T>G (NANS)
ENST00000495319.1:n.604T>G (NANS)
NM_018946.3:c.400T>G (NANS)	NP_061819.2:p.Ser134Ala
XM_011518787.1:c.52T>G (NANS)	XP_011517089.1:p.Ser18Ala
XM_011518788.1:c.24T>G (NANS)	XP_011517090.1:p.Asp8Glu
XM_011518787.2:c.52T>G (NANS)	XP_011517089.1:p.Ser18Ala
XM_011518788.2:c.24T>G (NANS)	XP_011517090.1:p.Asp8Glu
XM_017014811.1:c.-155T>G (NANS)	XP_016870300.1:n.-155T>G
XM_017015352.2:c.*29-4803A>C (TRIM14)	XP_016870841.1:n.*29-4803A>C
XM_024447574.1:c.52T>G (NANS)	XP_024303342.1:p.Ser18Ala
NM_018946.4:c.400T>G (NANS) MANE Select	NP_061819.2:p.Ser134Ala