Canonical Allele Identifier: CA2613918604

Gene: FADS2

Linked Data

• gnomAD v4: 11-61865729-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.61865733del , CM000673.2:g.61865733del	GRCh38
NC_000011.9:g.61633205del , CM000673.1:g.61633205del	GRCh37
NC_000011.8:g.61389781del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278840.9:c.*44del MANE Select	ENSP00000278840.4:n.*44del
ENST00000257261.10:c.*44del	ENSP00000257261.6:n.*44del
ENST00000278840.8:c.*44del	ENSP00000278840.4:n.*44del
ENST00000522056.5:c.*44del	ENSP00000429500.1:n.*44del
ENST00000523235.5:n.3459del
NM_001281501.1:c.*44del	NP_001268430.1:n.*44del
NM_001281502.1:c.*44del	NP_001268431.1:n.*44del
NM_004265.3:c.*44del	NP_004256.1:n.*44del
NM_004265.4:c.*44del MANE Select	NP_004256.1:n.*44del