Canonical Allele Identifier: CA1899187561

Gene: JCAD

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.30035003_30035005delinsGCA , CM000672.2:g.30035003_30035005delinsGCA	GRCh38
NC_000010.10:g.30323932_30323934delinsGCA , CM000672.1:g.30323932_30323934delinsGCA	GRCh37
NC_000010.9:g.30363938_30363940delinsGCA	NCBI36
NG_053080.1:g.85490_85492delinsTGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000375377.2:c.282-5139_282-5137delinsTGC MANE Select	ENSP00000364526.1:n.282-5139_282-5137deli...
ENST00000375377.1:c.282-5139_282-5137delinsTGC	ENSP00000364526.1:n.282-5139_282-5137deli...
NM_020848.2:c.282-5139_282-5137delinsTGC	NP_065899.1:n.282-5139_282-5137delinsTGC
XM_011519608.1:c.282-5139_282-5137delinsTGC	XP_011517910.1:n.282-5139_282-5137delinsT...
XM_011519609.1:c.-133-5139_-133-5137delinsTGC	XP_011517911.1:n.-133-5139_-133-5137delin...
XM_011519610.1:c.-133-5139_-133-5137delinsTGC	XP_011517912.1:n.-133-5139_-133-5137delin...
NM_001350001.1:c.-133-5139_-133-5137delinsTGC	NP_001336930.1:n.-133-5139_-133-5137delin...
NM_001350021.1:c.-133-5139_-133-5137delinsTGC	NP_001336950.1:n.-133-5139_-133-5137delin...
NM_001350022.1:c.282-5139_282-5137delinsTGC	NP_001336951.1:n.282-5139_282-5137delinsT...
NM_020848.3:c.282-5139_282-5137delinsTGC	NP_065899.1:n.282-5139_282-5137delinsTGC
NM_020848.4:c.282-5139_282-5137delinsTGC MANE Select	NP_065899.1:n.282-5139_282-5137delinsTGC
NM_001350001.2:c.-133-5139_-133-5137delinsTGC	NP_001336930.1:n.-133-5139_-133-5137delin...
NM_001350021.2:c.-133-5139_-133-5137delinsTGC	NP_001336950.1:n.-133-5139_-133-5137delin...
NM_001350022.2:c.282-5139_282-5137delinsTGC	NP_001336951.1:n.282-5139_282-5137delinsT...