Canonical Allele Identifier: CA589339397

Gene: NANS TRIM14

Linked Data

• dbSNP Id: rs1288542861
• gnomAD v2: 9-100839144-TAAC-T
• gnomAD v3: 9-98076862-TAAC-T
• gnomAD v4: 9-98076862-TAAC-T
• MyVariant Identifiers: chr9:g.100839145_100839147del (hg19) ; chr9:g.98076863_98076865del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076867_98076869del , CM000671.2:g.98076867_98076869del	GRCh38
NC_000009.11:g.100839149_100839151del , CM000671.1:g.100839149_100839151del	GRCh37
NC_000009.10:g.99878970_99878972del	NCBI36
NG_052789.1:g.25191_25193del

Transcript Alleles

HGVS	Amino-acid change
ENST00000210444.6:c.349-51_349-49del (NANS) MANE Select	ENSP00000210444.5:n.349-51_349-49del
ENST00000210444.5:c.349-51_349-49del (NANS)	ENSP00000210444.5:n.349-51_349-49del
ENST00000375098.7:c.*29-7178_*29-7176del (TRIM14)	ENSP00000364239.3:n.*29-7178_*29-7176del
ENST00000415280.1:c.-257_-255del (NANS)	ENSP00000404107.1:n.-257_-255del
ENST00000461452.1:n.2225_2227del (NANS)
ENST00000495319.1:n.553-51_553-49del (NANS)
NM_018946.3:c.349-51_349-49del (NANS)	NP_061819.2:n.349-51_349-49del
XM_011518787.1:c.1-51_1-49del (NANS)	XP_011517089.1:n.1-51_1-49del
XM_011518787.2:c.1-51_1-49del (NANS)	XP_011517089.1:n.1-51_1-49del
XM_017014811.1:c.-206-51_-206-49del (NANS)	XP_016870300.1:n.-206-51_-206-49del
XM_017015352.2:c.*29-4699_*29-4697del (TRIM14)	XP_016870841.1:n.*29-4699_*29-4697del
XM_024447574.1:c.-51_-49del (NANS)	XP_024303342.1:n.-51_-49del
NM_018946.4:c.349-51_349-49del (NANS) MANE Select	NP_061819.2:n.349-51_349-49del