Canonical Allele Identifier: CA1866767054

Gene: NANS TRIM14

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076780T= , CM000671.2:g.98076780T=	GRCh38
NC_000009.11:g.100839062T= , CM000671.1:g.100839062T=	GRCh37
NC_000009.10:g.99878883T=	NCBI36
NG_052789.1:g.25104T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.349-138T= (NANS) MANE Select	ENSP00000210444.5:n.349-138T=
ENST00000210444.5:c.349-138T= (NANS)	ENSP00000210444.5:n.349-138T=
ENST00000375098.7:c.*29-7093A= (TRIM14)	ENSP00000364239.3:n.*29-7093A=
ENST00000461452.1:n.2138T= (NANS)
ENST00000495319.1:n.553-138T= (NANS)
NM_018946.3:c.349-138T= (NANS)	NP_061819.2:n.349-138T=
XM_011518787.1:c.1-138T= (NANS)	XP_011517089.1:n.1-138T=
XM_011518787.2:c.1-138T= (NANS)	XP_011517089.1:n.1-138T=
XM_017014811.1:c.-206-138T= (NANS)	XP_016870300.1:n.-206-138T=
XM_017015352.2:c.*29-4614A= (TRIM14)	XP_016870841.1:n.*29-4614A=
XM_024447574.1:c.-138T= (NANS)	XP_024303342.1:n.-138T=
NM_018946.4:c.349-138T= (NANS) MANE Select	NP_061819.2:n.349-138T=