Canonical Allele Identifier: CA2690915348

Gene: NANS TRIM14

Linked Data

• gnomAD v4: 9-98076895-AGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076896_98076897del , CM000671.2:g.98076896_98076897del	GRCh38
NC_000009.11:g.100839178_100839179del , CM000671.1:g.100839178_100839179del	GRCh37
NC_000009.10:g.99878999_99879000del	NCBI36
NG_052789.1:g.25220_25221del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.349-22_349-21del (NANS) MANE Select	ENSP00000210444.5:n.349-22_349-21del
ENST00000210444.5:c.349-22_349-21del (NANS)	ENSP00000210444.5:n.349-22_349-21del
ENST00000375098.7:c.*29-7210_*29-7209del (TRIM14)	ENSP00000364239.3:n.*29-7210_*29-7209del
ENST00000415280.1:c.-228_-227del (NANS)	ENSP00000404107.1:n.-228_-227del
ENST00000461452.1:n.2254_2255del (NANS)
ENST00000495319.1:n.553-22_553-21del (NANS)
NM_018946.3:c.349-22_349-21del (NANS)	NP_061819.2:n.349-22_349-21del
XM_011518787.1:c.1-22_1-21del (NANS)	XP_011517089.1:n.1-22_1-21del
XM_011518787.2:c.1-22_1-21del (NANS)	XP_011517089.1:n.1-22_1-21del
XM_017014811.1:c.-206-22_-206-21del (NANS)	XP_016870300.1:n.-206-22_-206-21del
XM_017015352.2:c.*29-4731_*29-4730del (TRIM14)	XP_016870841.1:n.*29-4731_*29-4730del
XM_024447574.1:c.-22_-21del (NANS)	XP_024303342.1:n.-22_-21del
NM_018946.4:c.349-22_349-21del (NANS) MANE Select	NP_061819.2:n.349-22_349-21del