Canonical Allele Identifier: CA1866767254

Gene: NANS TRIM14

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076967G= , CM000671.2:g.98076967G=	GRCh38
NC_000009.11:g.100839249G= , CM000671.1:g.100839249G=	GRCh37
NC_000009.10:g.99879070G=	NCBI36
NG_052789.1:g.25291G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.398G= (NANS) MANE Select	ENSP00000210444.5:p.Gly133=
ENST00000210444.5:c.398G= (NANS)	ENSP00000210444.5:p.Gly133=
ENST00000375098.7:c.*29-7280C= (TRIM14)	ENSP00000364239.3:n.*29-7280C=
ENST00000415280.1:c.-157G= (NANS)	ENSP00000404107.1:n.-157G=
ENST00000461452.1:n.2325G= (NANS)
ENST00000495319.1:n.602G= (NANS)
NM_018946.3:c.398G= (NANS)	NP_061819.2:p.Gly133=
XM_011518787.1:c.50G= (NANS)	XP_011517089.1:p.Gly17=
XM_011518788.1:c.22G= (NANS)	XP_011517090.1:p.Asp8=
XM_011518787.2:c.50G= (NANS)	XP_011517089.1:p.Gly17=
XM_011518788.2:c.22G= (NANS)	XP_011517090.1:p.Asp8=
XM_017014811.1:c.-157G= (NANS)	XP_016870300.1:n.-157G=
XM_017015352.2:c.*29-4801C= (TRIM14)	XP_016870841.1:n.*29-4801C=
XM_024447574.1:c.50G= (NANS)	XP_024303342.1:p.Gly17=
NM_018946.4:c.398G= (NANS) MANE Select	NP_061819.2:p.Gly133=