Canonical Allele Identifier: CA938621953
Gene: FADS2 HGNC NCBI

Linked Data

dbSNP Id: rs2067159329

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.61834981_61834982insGCCCCCCC , CM000673.2:g.61834981_61834982insGCCCCCCC GRCh38
NC_000011.9:g.61602453_61602454insGCCCCCCC , CM000673.1:g.61602453_61602454insGCCCCCCC GRCh37
NC_000011.8:g.61359029_61359030insGCCCCCCC NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000278840.9:c.208-2797_208-2796insGCCCCCCC MANE Select ENSP00000278840.4:n.208-2797_208-2796insGCCCCCCC
ENST00000257261.10:c.142-2797_142-2796insGCCCCCCC ENSP00000257261.6:n.142-2797_142-2796insGCCCCCCC
ENST00000278840.8:c.208-2797_208-2796insGCCCCCCC ENSP00000278840.4:n.208-2797_208-2796insGCCCCCCC
ENST00000517312.5:c.-159-2797_-159-2796insGCCCCCCC ENSP00000430225.1:n.-159-2797_-159-2796insGCCCCCCC
ENST00000518606.5:c.-159-2797_-159-2796insGCCCCCCC ENSP00000430054.1:n.-159-2797_-159-2796insGCCCCCCC
ENST00000521849.5:c.208-2797_208-2796insGCCCCCCC ENSP00000431091.1:n.208-2797_208-2796insGCCCCCCC
ENST00000522056.5:c.115-2797_115-2796insGCCCCCCC ENSP00000429500.1:n.115-2797_115-2796insGCCCCCCC
NM_001281501.1:c.142-2797_142-2796insGCCCCCCC NP_001268430.1:n.142-2797_142-2796insGCCCCCCC
NM_001281502.1:c.115-2797_115-2796insGCCCCCCC NP_001268431.1:n.115-2797_115-2796insGCCCCCCC
NM_004265.3:c.208-2797_208-2796insGCCCCCCC NP_004256.1:n.208-2797_208-2796insGCCCCCCC
XM_011545395.1:c.208-2797_208-2796insGCCCCCCC XP_011543697.1:n.208-2797_208-2796insGCCCCCCC
NM_004265.4:c.208-2797_208-2796insGCCCCCCC MANE Select NP_004256.1:n.208-2797_208-2796insGCCCCCCC