Canonical Allele Identifier: CA869034541

Gene: NANS TRIM14

Linked Data

• dbSNP Id: rs1303362895
• MyVariant Identifiers: chr9:g.100839186_100839187del (hg19) ; chr9:g.98076904_98076905del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.98076905_98076906del , CM000671.2:g.98076905_98076906del	GRCh38
NC_000009.11:g.100839187_100839188del , CM000671.1:g.100839187_100839188del	GRCh37
NC_000009.10:g.99879008_99879009del	NCBI36
NG_052789.1:g.25229_25230del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000210444.6:c.349-13_349-12del (NANS) MANE Select	ENSP00000210444.5:n.349-13_349-12del
ENST00000210444.5:c.349-13_349-12del (NANS)	ENSP00000210444.5:n.349-13_349-12del
ENST00000375098.7:c.*29-7218_*29-7217del (TRIM14)	ENSP00000364239.3:n.*29-7218_*29-7217del
ENST00000415280.1:c.-219_-218del (NANS)	ENSP00000404107.1:n.-219_-218del
ENST00000461452.1:n.2263_2264del (NANS)
ENST00000495319.1:n.553-13_553-12del (NANS)
NM_018946.3:c.349-13_349-12del (NANS)	NP_061819.2:n.349-13_349-12del
XM_011518787.1:c.1-13_1-12del (NANS)	XP_011517089.1:n.1-13_1-12del
XM_011518787.2:c.1-13_1-12del (NANS)	XP_011517089.1:n.1-13_1-12del
XM_017014811.1:c.-206-13_-206-12del (NANS)	XP_016870300.1:n.-206-13_-206-12del
XM_017015352.2:c.*29-4739_*29-4738del (TRIM14)	XP_016870841.1:n.*29-4739_*29-4738del
XM_024447574.1:c.-13_-12del (NANS)	XP_024303342.1:n.-13_-12del
NM_018946.4:c.349-13_349-12del (NANS) MANE Select	NP_061819.2:n.349-13_349-12del