Canonical Allele Identifier: CA1866767103

Gene: NANS TRIM14

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076861A= , CM000671.2:g.98076861A=	GRCh38
NC_000009.11:g.100839143A= , CM000671.1:g.100839143A=	GRCh37
NC_000009.10:g.99878964A=	NCBI36
NG_052789.1:g.25185A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.349-57A= (NANS) MANE Select	ENSP00000210444.5:n.349-57A=
ENST00000210444.5:c.349-57A= (NANS)	ENSP00000210444.5:n.349-57A=
ENST00000375098.7:c.*29-7174T= (TRIM14)	ENSP00000364239.3:n.*29-7174T=
ENST00000415280.1:c.-263A= (NANS)	ENSP00000404107.1:n.-263A=
ENST00000461452.1:n.2219A= (NANS)
ENST00000495319.1:n.553-57A= (NANS)
NM_018946.3:c.349-57A= (NANS)	NP_061819.2:n.349-57A=
XM_011518787.1:c.1-57A= (NANS)	XP_011517089.1:n.1-57A=
XM_011518787.2:c.1-57A= (NANS)	XP_011517089.1:n.1-57A=
XM_017014811.1:c.-206-57A= (NANS)	XP_016870300.1:n.-206-57A=
XM_017015352.2:c.*29-4695T= (TRIM14)	XP_016870841.1:n.*29-4695T=
XM_024447574.1:c.-57A= (NANS)	XP_024303342.1:n.-57A=
NM_018946.4:c.349-57A= (NANS) MANE Select	NP_061819.2:n.349-57A=