Canonical Allele Identifier: CA2690915331

Gene: NANS TRIM14

Linked Data

• dbSNP Id: rs2117941947
• gnomAD v4: 9-98076866-AAC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076868_98076869del , CM000671.2:g.98076868_98076869del	GRCh38
NC_000009.11:g.100839150_100839151del , CM000671.1:g.100839150_100839151del	GRCh37
NC_000009.10:g.99878971_99878972del	NCBI36
NG_052789.1:g.25192_25193del

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.349-50_349-49del (NANS) MANE Select	ENSP00000210444.5:n.349-50_349-49del
ENST00000210444.5:c.349-50_349-49del (NANS)	ENSP00000210444.5:n.349-50_349-49del
ENST00000375098.7:c.*29-7181_*29-7180del (TRIM14)	ENSP00000364239.3:n.*29-7181_*29-7180del
ENST00000415280.1:c.-256_-255del (NANS)	ENSP00000404107.1:n.-256_-255del
ENST00000461452.1:n.2226_2227del (NANS)
ENST00000495319.1:n.553-50_553-49del (NANS)
NM_018946.3:c.349-50_349-49del (NANS)	NP_061819.2:n.349-50_349-49del
XM_011518787.1:c.1-50_1-49del (NANS)	XP_011517089.1:n.1-50_1-49del
XM_011518787.2:c.1-50_1-49del (NANS)	XP_011517089.1:n.1-50_1-49del
XM_017014811.1:c.-206-50_-206-49del (NANS)	XP_016870300.1:n.-206-50_-206-49del
XM_017015352.2:c.*29-4702_*29-4701del (TRIM14)	XP_016870841.1:n.*29-4702_*29-4701del
XM_024447574.1:c.-50_-49del (NANS)	XP_024303342.1:n.-50_-49del
NM_018946.4:c.349-50_349-49del (NANS) MANE Select	NP_061819.2:n.349-50_349-49del