Canonical Allele Identifier: CA1823684426

Gene: FAM135B

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.138491883_138491895delinsGTGCTGCTGAAGA , CM000670.2:g.138491883_138491895delinsGTGCTGCTGAAGA	GRCh38
NC_000008.10:g.139504126_139504138delinsGTGCTGCTGAAGA , CM000670.1:g.139504126_139504138delinsGTGCTGCTGAAGA	GRCh37
NC_000008.9:g.139573308_139573320delinsGTGCTGCTGAAGA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395297.6:c.-20+4776_-20+4788delinsTCTTCAGCAGCAC MANE Select	ENSP00000378710.1:n.-20+4776_-20+4788delinsTCTTCAGCAGCAC
ENST00000276737.10:c.-20+4776_-20+4788delinsTCTTCAGCAGCAC	ENSP00000276737.6:n.-20+4776_-20+4788delinsTCTTCAGCAGCAC
ENST00000395297.5:c.-20+4776_-20+4788delinsTCTTCAGCAGCAC	ENSP00000378710.1:n.-20+4776_-20+4788delinsTCTTCAGCAGCAC
NM_015912.3:c.-20+4776_-20+4788delinsTCTTCAGCAGCAC	NP_056996.2:n.-20+4776_-20+4788delinsTCTTCAGCAGCAC
XM_011517061.1:c.-165+4776_-165+4788delinsTCTTCAGCAGCAC	XP_011515363.1:n.-165+4776_-165+4788delinsTCTTCAGCAGCAC
XM_011517062.1:c.-20+4776_-20+4788delinsTCTTCAGCAGCAC	XP_011515364.1:n.-20+4776_-20+4788delinsTCTTCAGCAGCAC
NM_001362965.1:c.-20+5732_-20+5744delinsTCTTCAGCAGCAC	NP_001349894.1:n.-20+5732_-20+5744delinsTCTTCAGCAGCAC
XM_011517061.2:c.-165+4776_-165+4788delinsTCTTCAGCAGCAC	XP_011515363.1:n.-165+4776_-165+4788delinsTCTTCAGCAGCAC
NM_015912.4:c.-20+4776_-20+4788delinsTCTTCAGCAGCAC MANE Select	NP_056996.2:n.-20+4776_-20+4788delinsTCTTCAGCAGCAC
NM_001362965.2:c.-20+5732_-20+5744delinsTCTTCAGCAGCAC	NP_001349894.1:n.-20+5732_-20+5744delinsTCTTCAGCAGCAC