Canonical Allele Identifier: CA1866767496

Gene: NANS TRIM14

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98077195T= , CM000671.2:g.98077195T=	GRCh38
NC_000009.11:g.100839477T= , CM000671.1:g.100839477T=	GRCh37
NC_000009.10:g.99879298T=	NCBI36
NG_052789.1:g.25519T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.448+178T= (NANS) MANE Select	ENSP00000210444.5:n.448+178T=
ENST00000210444.5:c.448+178T= (NANS)	ENSP00000210444.5:n.448+178T=
ENST00000375098.7:c.*29-7508A= (TRIM14)	ENSP00000364239.3:n.*29-7508A=
ENST00000415280.1:c.-107+178T= (NANS)	ENSP00000404107.1:n.-107+178T=
ENST00000461452.1:n.2375+178T= (NANS)
ENST00000495319.1:n.652+178T= (NANS)
NM_018946.3:c.448+178T= (NANS)	NP_061819.2:n.448+178T=
XM_011518787.1:c.100+178T= (NANS)	XP_011517089.1:n.100+178T=
XM_011518788.1:c.71+179T= (NANS)	XP_011517090.1:n.71+179T=
XM_011518787.2:c.100+178T= (NANS)	XP_011517089.1:n.100+178T=
XM_011518788.2:c.71+179T= (NANS)	XP_011517090.1:n.71+179T=
XM_017014811.1:c.-107+178T= (NANS)	XP_016870300.1:n.-107+178T=
XM_017015352.2:c.*29-5029A= (TRIM14)	XP_016870841.1:n.*29-5029A=
XM_024447574.1:c.100+178T= (NANS)	XP_024303342.1:n.100+178T=
NM_018946.4:c.448+178T= (NANS) MANE Select	NP_061819.2:n.448+178T=