Canonical Allele Identifier: CA2229530545

Gene: NUTF2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.67868186_67868192delinsTGTTTGG , CM000678.2:g.67868186_67868192delinsTGTTTGG	GRCh38
NC_000016.9:g.67902089_67902095delinsTGTTTGG , CM000678.1:g.67902089_67902095delinsTGTTTGG	GRCh37
NC_000016.8:g.66459590_66459596delinsTGTTTGG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000568233.6:c.100-154_100-148delinsTGTTTGG	ENSP00000515099.1:n.100-154_100-148delins...
ENST00000569436.7:c.100-154_100-148delinsTGTTTGG	ENSP00000457989.1:n.100-154_100-148delins...
ENST00000570026.2:c.100-154_100-148delinsTGTTTGG	ENSP00000515106.1:n.100-154_100-148delins...
ENST00000700610.1:c.100-154_100-148delinsTGTTTGG	ENSP00000515098.1:n.100-154_100-148delins...
ENST00000700611.1:c.-150-154_-150-148delinsTGTTTGG	ENSP00000515101.1:n.-150-154_-150-148deli...
ENST00000700612.1:c.100-154_100-148delinsTGTTTGG	ENSP00000515102.1:n.100-154_100-148delins...
ENST00000700613.1:c.100-154_100-148delinsTGTTTGG	ENSP00000515103.1:n.100-154_100-148delins...
ENST00000700614.1:c.100-154_100-148delinsTGTTTGG	ENSP00000515104.1:n.100-154_100-148delins...
ENST00000700615.1:c.-150-154_-150-148delinsTGTTTGG	ENSP00000515105.1:n.-150-154_-150-148deli...
ENST00000219169.9:c.100-154_100-148delinsTGTTTGG MANE Select	ENSP00000219169.4:n.100-154_100-148delins...
ENST00000219169.8:c.100-154_100-148delinsTGTTTGG	ENSP00000219169.4:n.100-154_100-148delins...
ENST00000567105.5:c.100-154_100-148delinsTGTTTGG	ENSP00000456428.1:n.100-154_100-148delins...
ENST00000568233.5:n.180-154_180-148delinsTGTTTGG
ENST00000568390.5:n.192-154_192-148delinsTGTTTGG
ENST00000568396.2:c.100-154_100-148delinsTGTTTGG	ENSP00000457022.1:n.100-154_100-148delins...
ENST00000569436.6:c.100-154_100-148delinsTGTTTGG	ENSP00000457989.1:n.100-154_100-148delins...
ENST00000570026.1:n.244-154_244-148delinsTGTTTGG
NM_005796.1:c.100-154_100-148delinsTGTTTGG	NP_005787.1:n.100-154_100-148delinsTGTTTG...
XM_005255771.1:c.100-154_100-148delinsTGTTTGG	XP_005255828.1:n.100-154_100-148delinsTGT...
NM_001322038.1:c.100-154_100-148delinsTGTTTGG	NP_001308967.1:n.100-154_100-148delinsTGT...
NM_001322039.1:c.100-154_100-148delinsTGTTTGG	NP_001308968.1:n.100-154_100-148delinsTGT...
NM_001322040.1:c.100-154_100-148delinsTGTTTGG	NP_001308969.1:n.100-154_100-148delinsTGT...
NM_001322041.1:c.100-154_100-148delinsTGTTTGG	NP_001308970.1:n.100-154_100-148delinsTGT...
NM_005796.2:c.100-154_100-148delinsTGTTTGG	NP_005787.1:n.100-154_100-148delinsTGTTTG...
NM_005796.3:c.100-154_100-148delinsTGTTTGG MANE Select	NP_005787.1:n.100-154_100-148delinsTGTTTG...
NM_001322038.2:c.100-154_100-148delinsTGTTTGG	NP_001308967.1:n.100-154_100-148delinsTGT...
NM_001322039.2:c.100-154_100-148delinsTGTTTGG	NP_001308968.1:n.100-154_100-148delinsTGT...
NM_001322040.2:c.100-154_100-148delinsTGTTTGG	NP_001308969.1:n.100-154_100-148delinsTGT...
NM_001322041.2:c.100-154_100-148delinsTGTTTGG	NP_001308970.1:n.100-154_100-148delinsTGT...