Canonical Allele Identifier: CA2690915337

Gene: NANS TRIM14

Linked Data

• gnomAD v4: 9-98076881-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076881C>A , CM000671.2:g.98076881C>A	GRCh38
NC_000009.11:g.100839163C>A , CM000671.1:g.100839163C>A	GRCh37
NC_000009.10:g.99878984C>A	NCBI36
NG_052789.1:g.25205C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.349-37C>A (NANS) MANE Select	ENSP00000210444.5:n.349-37C>A
ENST00000210444.5:c.349-37C>A (NANS)	ENSP00000210444.5:n.349-37C>A
ENST00000375098.7:c.*29-7194G>T (TRIM14)	ENSP00000364239.3:n.*29-7194G>T
ENST00000415280.1:c.-243C>A (NANS)	ENSP00000404107.1:n.-243C>A
ENST00000461452.1:n.2239C>A (NANS)
ENST00000495319.1:n.553-37C>A (NANS)
NM_018946.3:c.349-37C>A (NANS)	NP_061819.2:n.349-37C>A
XM_011518787.1:c.1-37C>A (NANS)	XP_011517089.1:n.1-37C>A
XM_011518787.2:c.1-37C>A (NANS)	XP_011517089.1:n.1-37C>A
XM_017014811.1:c.-206-37C>A (NANS)	XP_016870300.1:n.-206-37C>A
XM_017015352.2:c.*29-4715G>T (TRIM14)	XP_016870841.1:n.*29-4715G>T
XM_024447574.1:c.-37C>A (NANS)	XP_024303342.1:n.-37C>A
NM_018946.4:c.349-37C>A (NANS) MANE Select	NP_061819.2:n.349-37C>A