Canonical Allele Identifier: CA869034884

Gene: NANS TRIM14

Linked Data

• dbSNP Id: rs1408463197
• gnomAD v3: 9-98077165-G-T
• gnomAD v4: 9-98077165-G-T
• MyVariant Identifiers: chr9:g.100839447G>T (hg19) ; chr9:g.98077165G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98077165G>T , CM000671.2:g.98077165G>T	GRCh38
NC_000009.11:g.100839447G>T , CM000671.1:g.100839447G>T	GRCh37
NC_000009.10:g.99879268G>T	NCBI36
NG_052789.1:g.25489G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.448+148G>T (NANS) MANE Select	ENSP00000210444.5:n.448+148G>T
ENST00000210444.5:c.448+148G>T (NANS)	ENSP00000210444.5:n.448+148G>T
ENST00000375098.7:c.*29-7478C>A (TRIM14)	ENSP00000364239.3:n.*29-7478C>A
ENST00000415280.1:c.-107+148G>T (NANS)	ENSP00000404107.1:n.-107+148G>T
ENST00000461452.1:n.2375+148G>T (NANS)
ENST00000495319.1:n.652+148G>T (NANS)
NM_018946.3:c.448+148G>T (NANS)	NP_061819.2:n.448+148G>T
XM_011518787.1:c.100+148G>T (NANS)	XP_011517089.1:n.100+148G>T
XM_011518788.1:c.71+149G>T (NANS)	XP_011517090.1:n.71+149G>T
XM_011518787.2:c.100+148G>T (NANS)	XP_011517089.1:n.100+148G>T
XM_011518788.2:c.71+149G>T (NANS)	XP_011517090.1:n.71+149G>T
XM_017014811.1:c.-107+148G>T (NANS)	XP_016870300.1:n.-107+148G>T
XM_017015352.2:c.*29-4999C>A (TRIM14)	XP_016870841.1:n.*29-4999C>A
XM_024447574.1:c.100+148G>T (NANS)	XP_024303342.1:n.100+148G>T
NM_018946.4:c.448+148G>T (NANS) MANE Select	NP_061819.2:n.448+148G>T